Professional Documents
Culture Documents
BIOTIN. I. 2-ALKYLTHIOPHANE-3,4-DICARBOXYLIC
ACIDS
B. R.BAKER, MERLE V. QUERRY,S.R. SAFIR, AND SEYMOUR BERNSTEIN
I 3
0 0 0
I
I- /I
/E
\S,
-+
IV
0
HO '
CN
COOR' HO '
COOH
COOH
kLR __3
v [I VI11 Lx
J.
COKHNH2
I
h
\ S,,-R
Co""2
XI1
(1) CHIN,
(2) N2H4 uIooH
COOH
I
XI
c--
COOH
x
i
"COO
r', , I-ICOOC8H6
I
CaHs
( 1 ) soc12
t (2) NaNI
(3) CzHoOH
XI11
a series R = 72-C3H7-, R' = CaH6-
b series R = CBHLO-(CHa)a-,R' = CH3-
crystalline isomer, m.p. 156-157", was easily isolated, due to its insolubility in
benzene.
The crystalline isomer was shown to have its carboxyl groups related by a
140 BAKER, QUERRY, SAFIR, AND BERXSTEIN
trans configuration as (a) it was stable to heat at 250"; (b) it gave a diacid chloride
with thionyl chloride; (c) it formed a mixed anhydride when treated with acetyl
chloride and the same acid was regenerated on hydrolysis; (d) it was converted
with boiling propionic anhydride t o a mixture of isomeric cis anhydrides from
which a crystalline cis diacid, m.p. 130-131", could be isolated. The carboxyl
groups of the latter have a cis configuration as (a) acetyl chloride or thionyl
chloride gave an inner anhydride which regenerated the same acid on treatment
with water; (b) it evolved water a t 150" to form an anhydride; (c) it formed a
cyclic imide. Thus, two of the possible four racemic modifications of 2-propyl-
thiophane-3,4-dicarboxylicacid (XIa) have been characterized, one cis and one
trans.
The preparation of 2-(yphenoxypropyl)thiophane-3,4-carboxylicacid (XIb)
followed the same reactions except that dehydration of the hydroxy acid, IXb,
was accomplished by means of boiling acetic anhydride. Again a trans diacid,
m.p. 183", was readily separated and mas convertible to the cis anhydrides with
boiling propionic anhydride. One of the cis anhydrides, m.p. 105", was isolated
and hydrolyzed to a cis diacid, m.p. 158". The cis and trans configurations were
established in the same manner as for the 2-propylthiophane-3 ,4-dicarboxylic
acids (XIa).
2-(y-Phenoxypropyl)thiophane-3,4-trans-dicarboxylic acid (XIb) was prepared
by a second method. yPhenoxypropylmalonic acid (XIV) on chlorination with
sulfuryl chloride followed by decarboxylation gave a mixture of 5-phenoxyvaleric
acid, 5-chlorophenoxyvaleric acid, 2-chloro-5-phenoxyvaleric acid (XVI), and
2-chloro-5-chlorophenoxyvalericacid. The mixture was treated with sodium
hydrosulfide, then esterified. Cold alkaline extraction of a n ethereal solution of
the esters gave on acidification a mixture of methyl 2-mercapto-5-phenoxyval-
erate (XVIII) and methyl 2-mercapto-5-chlorophenoxyvalerate,which mere
separated by fractional distillation, in yields of 14% and 8% respectively based
on the original malonic acid, XIV.
Condensation of the methyl 2-mercapto-5-phenoxyvalerate(XTTIII) with
methyl acrylate in the presence of piperidine followed by Dieckmann cyclization
with sodium methoxide in ether proceeded smoothly t o 2-(yphenoxypropy1)-3-
keto-4-carbomethoxythiophane (XIX). In this case the Dieckmann reaction
can take place only as indicated, as formation of the isomeric 2-(y-phenoxy-
propyl)-2-carbomethoxy-3-ketothiophane would involve the elimination of
methanol between a carbomethoxy group and a tertiary hydrogen, which takes
place only with difficulty (4).
The keto ester, XIX,3 was converted to 2-(r-phenoxypropyl)thiophane-3,4-
trans-dicarboxylic acid by the same series of reactions used for the isomeric
2-(y-phenoxypropyl)-3-carbomethoxy-4-ketothiophane(Vb). The crystalline
trans acids obtained by both methods were identical, thus offering additional
proof of the direction of ring closure in the preparation of the keto ester, Vb.
The yield of crystalline trans diacid, m.p. 183", obtained on sodium amalgam
* After this work was completed Cheney and Piening (20) published 8 superior method
for the preparation of the corresponding keto ethyl ester.
BIOTIN. I 141
reduction of XXII, was 29%. The isomers in the filtrate were esterified, treated
with sodium methoxide to invert cis isomers to trans and then hydrolyzed. An-
other 20% of the same crystalline trans acid was obtained. The filtrate from
this material presumably contained a second trans isomer which did not crystal-
lize. It was boiled with propionic anhydride in order to invert it back to the cis
isomers, then esterified and reinverted back to the trans isomers by treatment
COOH COOH
I I
CaHsO (CHJSCHCOOH +
SOzclr CeHaO(CH2)3CCOOH ---+
I
c1
XIV xv
COOH COOH
1
COOH COOH
XXII XIb
with sodium methoxide. In this way an additional 7%, a total of 56%) of the
crystalline trans isomer was ~ b t a i n e d . ~
4 Since completion of this work, Grussner, Bourguin, and Schnider (21) have described
The trans dicarboxylic acids, XI, were converted via the methyl esters to the
trans dihydrazides, XII, which were in turn degraded by the Curtius method to
the trand diurethans. The 2-(-y-phenoxypropyl)-3,4-trans-dicarbethoxylamino-
thiophane (XIIIb) was prepared more easily and in better yield by treating the
diacid chloride of the trans dicarboxylic acid, XI, with sodium azide in dilute
acetone (6). However, when the esters of 2-propyl- or 2-(y-phenoxypropyl)-
thiophane-3 ,4-cis-dicarboxylic acids were treated with hydrazine under a variety
of conditions, no cis dihydrazides6 could be isolated, but inversion to the trans
dihydrazides, XII, took place. Similarly when the imide (XXIII) or cyclic
hydrazide (XXIV) of 2-propylthiophane-3 4-cis-dicarboxylic acid was treated
)
with hydrazine, the trans dihydrazide, XIIa, was formed. Apparently hydrazine
is sufficiently alkaline to cause rearrangement of a cis diester or cis dihydrazide
t o the more stable trans configuration by enolization of the carbonyl groups in the
same manner as sodium niethoxide.
NH NH-NH
/ \ I I
co co CO"", co co
CONHNHi
t-
OC&I, ----$ b C &
XIIIb xxv
I
XXVIII
EXPERIMENTAL
Butylideneacetonitrile (11). A mixture of 75 g. of butylidenecyanoacetic acid ( l l ) , 75
cc. of quinoline, and 0.8 g. of copper oxide was heated in a 250 cc. modified Claisen flask
at 125-140" (bath) for twenty-five minutes, when the evolution of carbon dioxide had
practically ceased. The product was distilled out of the reaction mixture a t 15 mm. until
the vapors reached 110". Redistillation gave in four runs 23.5-24.3 g. (4648%) of a water-
white liquid, b.p. 57-59" (12 mm.).
Letch and Linstead (11) decarboxylated this acid by heating its mixture with sand, and
7 Bennet and Hock (22) have observed a similar type of ring closure on hydrobromic
acid hydrolysis of bis-(6-benzyloxybutyl) sulfide. The product was l-(t-hydroxybutyl)-
thiophanium bromide and no bis-(t-bromobutyl) sulfide could be isolated.
144 BAKER, QUERRY, SAFIR, AND BERNSTEIN
reported that the yield vaned widely and never exceeded 40%. They record the boiling
point 57-58' (11 mm.).
Ethyl thioglycolate. A mixture of 150 g. of thioglycolic acid, 200 cc. of absolute ethanol,
300 cc. of benzene, and 20 cc. of concentrated sulfuric acid was refluxed for sixteen hours
under a Soxhlet apparatus containing about 90 g. of anhydrous magnesium sulfate in the
thimble. The cooled mixture was washed twice with water, solvent removed through a
Vigreux column, and the residue distilled; colorless liquid, b.p. 63' (20 mm.); yield, 174 g.
(89yo). If water is not continuously removed, as in the ordinary esterification, the yield is
about 60%.
The methyl ester may be prepared similarly using methanol and chloroform; yield,
7742%.
This method (12) is used routinely for all esterifications of this type and has been found
to give invariably higher yields than can be obtained without continuous drying.
Methyl 8-hezenoate. 2-Hexenoic acid was prepared from n-butyraldehyde and malonic
acid according to Goldberg and Linstead (13), except that a 25% excess of aldehyde was
employed and the reaction was allowed to proceed for seventeen hours a t room temperature;
yield, 76% of product, m.p. 32'.
From 278 g. of 5-hexenoic acid, 300 cc. of methanol, 300 cc. of chloroform, and 30 cc. of
concentrated sulfuric acid, using 90 g. of anhydrous magnesium sulfate for continuous
drying as described above, was obtained 305 g. (98%) of the ester, b.p. 56-58' (13 mm.).
The ethyl ester was prepared in the same manner using ethanol and benzene, b.p. 72-73'
(15 mm.); yield, 94%.
The esterification reaction of 2-hexenoic acid has been found by Thomas and Sudborough
(14) to be sensitive t o water and they have shown that at equilibrium only 15% of the methyl
ester is formed. The only esterification of this acid reported in the literature is that of
Kon, Linstead, and MacLennan (15) who treated the silver salt with ethyl iodide. They
record the b.p. 80" (22 mm.).
Methyl 6-phenozy-2-hezenoate (IIIb). From 46 g. of 6-phenoxy-2-hexenoic acid (23),
5 cc. of concentrated sulfuric acid, 100 cc. of methanol, and 100 cc. of chloroform was ob-
tained 42 g. (86%) of the ester by the continuous drying procedure; b.p. 135-138" (1 mm.).
Anal. Calc'd for C13H1603: C, 70.8; H, 7.3.
Found: C, 70.4; H , 6.8,
2-Propyl-S-cyano-~-ketothiophane( I V a ) . To the dry sodium ethoxide from 8.3 g. of
sodium and 150 cc. of absolute ethanol, obtained by evaporating the solution to dryness
in vacuo, was added in a nitrogen atmosphere a solution of 42.5 g. of ethyl thioglycolate in
60 cc. of benzene. After most of the sodium ethylate had dissolved, a solution of 37.2 g.
of butylideneacetonitrile in 30 cc. of benzene was added. The solution was refluxed for
one hour on the steam-bath, during which the sodium salt of the product separated. The
cooled mixture was extracted with ice-water, the extracts immediately acidified, and the
oil which separated a a s extracted with benzene. Distillation gave 31 g. (52%) of a yellow
oil, b.p. 125-127' (1 mm.), n f 1.5118.
Anal. Calc'd for CSH11NOS: C, 56.7; H, 6.5; K, 8.3.
Found: C , 56.4; H , 6.3; N, 7.8.
The semicarbazone formed white crystals from dilute alcohol, m.p. 175-176'.
Anal. Calc'd for C ~ H I A N ~ O C,S47.8;
: H, 6.2; N, 24.8.
Found: C, 48.1; H, 6.1; N, 25.2.
2-Propyl-8-carbethoxy-4-ketothiophane (Vu). A . A mixture of 15 g. of 2-propyl-3-cyano4
ketothiophane (IVa) in 7 cc. of absolute alcohol was treated with dry hydrogen chloride
until 3.3 g. had been absorbed. After two days in a stoppered flask, the mixture was diluted
with water and benzene and stirred for twenty hours. The separated benzene layer was
extracted twice with iced 5% sodium hydroxide and the extracts immediately acidified with
acetic acid. The oily layer was taken up in benzene, then distilled, b.p. 108-111" (1 mm.),
n: 1.4927; yield, 9 g. (47%).
BIOTIN. I 145
cc. of water, and 63 cc. of concentrated sulfuric acid for twelve hours, then diluted t o 2 1.
with water. The oil was taken up in ethyl acetate and extracted with aqueous sodium
bicarbonate solution. The ethyl acetate layer was washed with water and evaporated.
The residue consisted of 10.5 g. (22%) of crude 2-(~-phenoxypropyl) -4-ketothiophane
(VIIb), which was purified as previously described.
The sodium bicarbonate solution of acidic material was acidified, the oil extracted with
ethyl acetate, and the latter washed twice with water containing a little salt.8 Evaporation
of the ethyl acetate in vacuo gave 40 g. (60%) of product as a gummy mixture of stereoiso-
mers which was used in the next step without further purification.
One of the isomers crystallized when a benzene solution of the mixture was allowed t o
stand. It was purified by recrystallization from ethylene dichloride-acetone, then dilute
acetic acid, white crystals, m.p. 200-202' dec.
Anal. Calc'd for ClsHlaOeS: C, 55.2;H, 5.5.
Found: C,55.2; H, 5.1.
When the cyanohydrin, VIIIb, was hydrolyzed with hydrochloric acid in acetic acid in
the same manner as described for 2-propyl-3-carbethoxy4-hydroxy~-cyanothiophane
(VIIIa), no product could be isolated except small amounts of phenol.
i?-PropyEdihydrothiophene-S,8-dicarboxylic acid ( X a ) and anhydride. A mixture of 19 g.
of 2-propyl4-hydroxythiophane-3,4-dicarboxylic acid (IXa) and 0.1 cc. of 85% phosphoric
acid was distilled a t 2-8 mm. and a bath temperature of 190-210". Redistillation gave 11.1
g. of an oil, b.p. 125-145' (1mm.). Analyses indicated a mixture of the acid and anhydride.
About the same results were obtained when 1 g. of potassium bisulfate was substituted for
the phosphoric acid.
A mixture of 9.5 g. of the above distillate, 2 cc. of concentrated sulfuric acid, 40 cc. of
methanol, and 60 cc. of chloroform was refluxed overnight with continuous drying in the
usual manner. The 2-propyl-3,4-dicarbomethoxydihydrothiophenewas obtained as an
oil, b.p. 123-125' (1mm.), n: 1.5018;yield, 8.4g. (72%).
Anal. Calc'd for C,,H,aOS: C, 54.2; H, 6.6.
Found: C, 54.2; H, 5.8.
A crystalline acid, m.p. 150-152', was obtained by treatment of the pyrolysis distillate
with water followed by crystallization from benzene.
Anal. Calc'd for C O H ~ ~ OC, & :50.0; H, 5.6.
Found: C, 50.4;H, 5.4.
7-Phenozypropylmalonic acid ( X I V ) . This acid, prepared by methods described in the
literature (17), has been reported as melting indefinitely between 70" and 100". This has
been found to be due t o water of crystallization. The anhydrous material can be obtained
by refluxing its solution in benzene, with or without the addition of ethyl acetate t o aid
solubility, under a constant water separator until no more water is removed. On cooling,
the solution deposits crystals of the anhydrous acid, m.p. 113-114' (20).
Anal. Calc'd for C12Hl406:C, 60.4;H, 5.9.
Found: C,60.2;H, 5.5.
Methyl 2-mercapto-6-phenoxyvalerate( X V I I I ) . To a refluxing solution of 160 g. of m h y -
drous 7-phenoxypropylmalonic acid (XIV) in 640 cc. of chloroform was added dropwise
over a period of twenty minutes 57 cc. of sulfuryl chloride. After being refluxed for ninety
minutes more, the solution was evaporated t o dryness in vacuo. The residue waa heated
with 1.6 g. of copper oxide at 145-160" until carbon dioxide evolution was complete which
required twenty-five minutes.
The cooled residue was dissolved in 400 cc. of water containing 37 g. of anhydrous sodium
carbonate and added to a solution of 54 g. of sodium hydroxide in 280 cc. of water saturated
with hydrogen sulfide. After being heated on the steam-bath for ninety minutes, the solu-
tion was poured into a mixture of ice and 200 cc. of concentrated hydrochloric acid. The
-~ ~~
8I t is necessary to remove inorganic acids from the crude hydroxy acid, as traces cause
acetylation instead of dehydration by acetic anhydride in the next step.
148 BAKER, QUERRY, SAFIR, AND BERNSTEIN
viscous oil was extracted with two 200-cc. portions of chloroform. The extracts were
diluted with 200 cc. of methanol and 5 cc. of concentrated sulfuric acid, then refluxed for
about fifteen hours under a Soxhlet apparatus containing anhydrous magnesium sulfate
in the thimble. The solution, concentrated to turbidity in vacuo, was diluted with 500 cc.
of ice-water and the esters extracted with ether. The latter was extracted with two 500-cc.
portions of iced 3% sodium hydroxide and the extracts immediately run into iced hydro-
chloric acid. The mercaptans were extracted with benzene, washed with aqueous sodium
bicarbonate and water, then the solvent was evaporated. The residue was fractionated
through a Widmer column. The product (XVIII) was obtained as a colorless oil, b.p.
138-142' (1 mm.); yield, 22 g. (14%).
Anal. Calc'd for C ~ ~ H t 6 0C,~ S59.9;
: H, 6.7.
Found: C , 59.7; H, 7.1.
The second fraction, b.p. 155-158" (1 mm.), consisted of 15 g. (8%) of methyl 2-mercapto-
5-chlorophenoxyvalerate.
Anal. Calc'd for C12H1&103S:C, 52.3; H, 5.5.
Found: C, 52.3; H, 5.6.
A large number of variations of the halogenation were tried without increasing the yield.
Bromine gave about the same yields as sulfuryl chloride.
Z-(y-Phenoxypropyl)-3-keto-~-carbomethoxythiophane( X I X ) . To a mixture of 25.3 g.
of methyl 2-mercapto-5-phenoxyvalerate(XVIII) and 0.2 cc. of piperidine was added 13
cc. of methyl acrylate, in portions with ice cooling, so that the temperature was 40-45".
After five hours at room temperature, the mixture was dissolved in 150 cc. of dry ether and
added to the dry sodium methoxide obtained by evaporating t o dryness in vacuo a solution
of 2 g. of sodium in methanol. The sodium methoxide rapidly dissolved on swirling. The
solution, after sixteen hours a t room temperature protected from moisture, was extracted
three times with ice-water, the extracts being immediately run into iced hydrochloric acid.
The oil was extracted with benzene, washed with aqueous sodium bicarbonate and water.
Removal of the solvent in vacuo left the keto ester as a yellow-orange oil; yield, 22.7 g.
(73%). The keto ester gave a purple color with alcoholic ferric chloride.
Anal. Calc'd for ClaH1804S: C, 61.3; H, 6.2.
Found: C, 61.0; H, 6.5.
The semicarbazone was prepared in dilute methanol and recrystallized from aqueous
acetone; urhite crystals, m.p. 160-161".
Anal. Calc'd for CleH21NsO~:C, 54.7; H, 6.0; N, 11.9.
Found: C, 55.0; H, 6.7; K, 11.8.
8-(y-Chlorophenoxypropyl)-J-keto-~-carbomethoxythiophane.Prepared from methyl
2-mercapto-5-chlorophenoxyvaleratein the same manner as described for XIX, it was a n
orange oil. The semicarbazone formed white crystals, m.p. 181-182", when recrystallized
from dilute acetone.
Anal. Cslc'd for Cl~H~oClN30aS: C, 50.3; H, 5.2; N, 10.9.
Found: C, 50.4; H, 5.6; K, 10.3.
2-(y-Phenoxypropyl) -3-hydroxythiophane-3,Q-dicarboxylic acid ( X X I ). 2-(y-Phenoxy-
propyl)-3-keto-4-carbomethoxythiophane(XIX) was converted t o the cyanohydrin and
hydrolyzed with 20% sulfuric acid containing no acetic acid in the same manner as for the
isomeric hydroxy acid, IXb. The mixture of isomers, obtained in 71% yield, did not
crystallize.
Anal. Calc'd for C15H180eS: C, 55.2; H, 5.5.
Found: C, 55.0; H, 5.6.
The intermediate cyanohydrin, XX, was also analyzed.
Ana2. Calc'd for ClaHl&OaS: N, 4.4. Found: N, 3.9.
b-(y-Phenoxypropyl)dihydro~hiophene-3,~-d~carboxylic acid. Preparation of X b . A
mixture of 67 g . of 2-(y-phenoxypropyl)-4-hydroxythiophane-3,4-dicarboxylic acid isomers
(IXb) and 330 cc. of acetic anhydride was refluxed for two hours. Most of the acetic anhy-
dride was removed i n vacuo and the residue heated on the steam-bath with 900 cc. of water
BIOTIN. I 149
for twenty minutes with occasional shaking. The oily acid was extracted with ethyl
acetate, washed with dilute hydrochloric acid, and extracted in turn with aqueous sodium
bicarbonate. Acidification gave an oil which was extracted with ethyl acetate. The
extracts, dried with anhydrous sodium sulfate and clarified with Norit, were evaporated
in vacuo to give 54 g. (85%) of an amber gum.
One of the isomers was obtained crystalline from benzene and was purified by recrystalli-
zation from the same solvent, white crystals, m.p. 133-136".
-4naE. Calc'd for C15Hl,0jS: C, 58.4;H, 5.2.
Found: C. 58.6;H, 4.7.
Preparation of X X I I . From 23.1 g. of 2-(r-phenoxypropyl)-3-hydroxythiophane-3,4-
dicarboxylic acid (XXI) and 120 cc. of acetic anhydride in the same manner as above was
obtained 16.8g. (77%) of an oily, somewhat impure product satisfactory for the next step.
A n d . Calc'd for C1jHl6O5S:C, 58.4;H, 5.2.
Found: C, 57.8;H, 5.8.
2-Propylthiophane-J,~-trans-dicarboxylic acid ( X I a ) . A mixture of 10 g. of 2-propyl-
dihydrothiophene-3,4-dicarboxylicacid (Xa) and its anhydride was warmed with 42 cc. of
10% sodium hydroxide and 55 cc. of water until solution was complete. The solution was
stirred with 150 g. of 2% sodium amalgam at a bath temperature of 70-75" for two hours.
The solution, decanted from the mercury, was acidified and the oil extracted with chloro-
form. The solvent was evaporated and the residue crystallized from benzene-heptane at
0'. The solid was collected on a filter and washed with benzene; yield, 2.9 g. (26%), m.p.
148-153'. For analysis a sample was purified by recrystallization from benzene containing
a little acetone, white crystals, m.p. 156-157" which evolve no gas up to 250".
Anal. Calc'd for C8H1104S:C, 49.5;H, 6.4.
Found: C, 49.6,49.8; H, 5.9,5.9.
X-(~-Phenoxypropyl)thiophane-J,~-trans-dicarbozylic acid ( X I b ) . A . A solution of 54 g.
of 2-(~-ph~noxypropyl)dihydrothiophene-3,4-dicarboxylic acid (Xb) in 350 cc. of water
containing 15 g. of sodium hydroxide was stirred with 540 g. of 2% sodium amalgam in the
same manner as described for the corresponding propyl compound, XIa, except that ethyl
acetate was used for extraction. The crystalline trans acid was obtained when the mixture
of isomers was triturated n-ith benzene, yield, 16.6g. (31%), m.p. 169-175'. Recrystalliza-
tion from acetone-ethylene dichloride gave white crystals, m.p. 182-183'.
A n d . Calc'd for C l ~ H l ~ OC,
~ S58.1;
: H, 5.8.
Found: C,58.0;H, 5.5.
B . A solution of 16.8 g. of 2-(~-phenoxypropyl)dihydrothiophene-3,4-dicarboxylic acid
(XXII) in dilute alkali was reduced with sodium amalgam in the same manner as A : yield,
4.9 g. (29%), m.p. 175-178'. A mixed m.p. with preparation A was 179-181'.
The benzene filtrate (about 100 cc.) was diluted with 50 cc. of absolute ethanol and 1 cc.
of concentrated sulfuric acid and refluxed for fifteen hours under a Soxhlet apparatus con-
taining anhydrous magnesium sulfate in the thimble. The solution was washed with water
and evaporated in z'acuo. The residual diester was refluxed with 50 cc. of 1% methanolic
sodium methoxide for two hours, then diluted with 10 g. of potassium hydroxide in 100 cc.
of water and refluxed three hours more. Most of the methanol was evaporated, the solution
diluted with water, acidified, and extracted with ethyl acetate. The ethyl acetate extract
was worked up in the same manner as above. An additional 3.4 g. (20%) of trans diacid,
m.p. 172-17S0was obtained. A mixture with preparation A melted a t 175-180'.
The benzene filtrate was evaporated. The residue consisted of 7 g. of an oil which was
prohably mainly the second trans isomer. It was refluxed with 35 cc. of propionic anhydride
for t,wo hours and the excess anhydride removed in vacuo. The residue was converted t o
the dimethyl ester by the previously described continuous drying method. The dimethyl
ester was then distilled in a two-bulbed distilling flask at 1 mm., b.p. 180-220". The di-
methyl ester was rearranged and hydrolyzed t o the trans acids as above. Crystallization
from benzene gave 1.2 g. (7%) of trans acid, m.p. 175-180". A mixed m.p. with preparation
A was 178-181".
150 BAKER, QUERRY, SAFIR, AND BERNSTEIN
Thus, the total yield of one crystalline trans isomer in this reduction was 56%.
I-Propylthiophane-S,4-cis-dicarboxylic acid (XZu). A solution of 1.07 g. of the corre-
sponding crystalline trans acid in 5 cc. of propionic anhydride was refluxed for two hours,
then the excesa anhydride was distilled in vucuo. The residue was warmed with 10% aque-
ous sodium hydroxide until solution was complete. The solution, acidified and saturated
with salt, was extracted with ethyl acetate. Removal of the ethyl acetate in vacuo left
an oil which was crystallized from carbon tetrachloride, yield, 0.61 g. (57%) in two crops,
m.p. 127-129" and evolving gas when heated to 150". Recrystallization from carbon tetra-
chloride-petroleum ether gave white crystals, m.p. 130-131".
Anal. Calc'd for CBHIIO~S: C, 49.5;I€, 6.4.
Found: C, 49.2;H, 6.6.
2-(~-Phenoxypropyl)thiophane-S,~-cis-dicarboxylic anhydride. A solution of 500 mg. of
2-(~-phenoxypropyl)thiophane-3,4-trans-dicarboxylic acid (XIb, m.p. 182-183") in 2.5 cc.
of acetic anhydride was refluxed for three hours and the solvent was evaporated in vacuo.
The residue was distilled in a two-bulbed distilling flask a t 1 mm. The distillate partially
crystallized. Recrystallization from benzene-petroleum ether gave 240 mg. of white crys-
tals, m.p. 90-98". Further recrystallization raised the m.p. to 104-105".
Anal. Calc'd for ClsHleO8: C, 61.7;H, 5.5.
Found: C, 62.4;H , 5.3.
2-(~-Phenoxypropyl)tl~iophaneS,~-czs-dicurboxylic aczd ( X l b ) . A. A warm solution of
50 mg. of pure 2-(~-phenoxypropyl)thiophane-3,4-cis-dicarboxylicanhydride in 10%
aqueous sodium hydroxide was acidified. White crystals separated, m.p. 157-158", and
evolved gas at 190'. The m.p. was unchanged on recrystallization from acetone-benzene-
petroleum ether.
Anal. Calc'd for C15H1805S: C , 58.1;H, 5.8.
Found: C, 58.2;H , 5.2.
B. A mixture of 22.8 g. of 2-(~-phenoxypropyl)thiophane-3,4-trans-dicarboxyIic acid
(XIb, m.p. 169-175') and 160 cc. of propionic anhydride was refluxed for two hours, then
excess anhydride removed m vucuo. The residue was warmed with 10% aqueous sodium
hydroxide until solution was complete, treated with Norit, and acidified. The oil was
extracted v,Tith ethyl acetate, the extract washed with dilute hydrochloric acid, and the
solvent evaporated in vacuo. Trituration of the partially crystalline residue with hot ben-
zene gave 7.7 g. (34%) of white crystals, m.p. 134-156'. The filtrate, on standing overnight,
deposited 2.9 g. (13%) of crystals, m p. 140-143".
The czs diacid, when converted to the methyl ester with diazomethane and boiled with
methanolic sodium methoxide, then hydrolyzed with potassium hydroxide, gave the trans
diacid, m.p. and mixed m.p. 183-184'.
2-Propylthiophane-S,4-trans-dicarboxh1~dra~ide ( X I I a ). A , To a suspension of 2 g. of
2-propylthiophane-3,4-trans-dicarboxylic acid (XIa) in 20 cc. of ether was added an excess
of ethereal diazomethane. The oily ester remaining after evaporation of th2 ether was
refluxed with 15 cc. of methanol and 2 cc. of 55% hydrazine hydrate for one hour. Evap-
oration in vacuo gave 2.1 g. (94%) of product, m.p. 225" dec. Recrystallization from 50%
alcohol gave white crystals, m.p. 234" dec.
Anal. Calc'd for C9H18S10LS:C, 43.8;H, 7.4;N,22.7.
Found: C, 44.1;H , 6.7;N,22.4.
The configuration of the trans dihydrazide was demonstrated by hydrolysis with 6 N
hydrochloric acid back t o 2-propylthiophane-3,4-trans-dicarboxylicacid (XIa), m.p.
152-154". A mixed m.p. was 154-156'.
B. A mixture of 1.05 g. of 2-propyl-3,4-cis-dicarbomethoxythiophane and 0.6 cc. of 100%
hydrazine hydrate was heated on the steam-bath under reflux for one hour. Trituration
with alcohol gave 0.47 g. (45%) of the trans dihydrazide, m.p. 203-210" dec.
A large number of experiments were run under various conditions of time, temperature,
and solvents, but no cis dihydrazide was isolated. The only product which could be ob-
tained was the trans dihydrazide in yields varying from 15% to 50% and melting points from
BIOTIN. I 151
203" to 230" dec. The identity with trans dihydrazide was ehown by mixed melting points
in each case.
~-(~-Phenoxypropyl)thiophane-3,4-trans-dicarboxhydrazide (XIIb). A. A suspension of
350 mg. of 2-(-y-phenoxypropyl)thiophane-3,4-trans-dicarboxylic acid (XIb) in ether was
treated with an excess of ethereal diazomethane. Evaporation left a crystalline methyl
ester. It was refluxed for five hours with 10 cc. of Cellosolve and 0.4 cc. of 85% hydrazine
hydrate. Removal of the solvent left the crystalline hydrazide which was triturated with
benzene; yield, 300 mg. (7979,m.p. 202-204" after recrystallization from aqueous propanol.
Anal. Calc'd for C I ~ I ~ ~ ~ NK, S S : Found: N, 16.5.
~ O16.6.
When the trans dihydrazide was heated at 100" for twenty hours with 10% sulfuric acid,
the zrans diacid (XIb) separated, m.p. and mised m.p. 181-183".
B. The dimethyl ester prepared from 0.47 g. of 2-(-pphenoxypropyl)thiophane-3,4-cis-
dicarboxylic acid, (XIb) and excess ethereal diazomethane was refluxed with 0.9 cc. of 85%
hydrazine hydrate for six hours (bath 130-135"). The cooled mixture was triturated with
methanol; yield, 0.17 g. (34%), m.p. 197-204". A mixed m.p. with preparation A showed
them t o be identical.
No crystalline product other than the trans dihydrazide could be isolated by shorter
heating periods with or without solvents.
2-Propyl-J,~-trans-dicarbethoxyaminothiophane (XIIIa). To a solution of 0.50 g. of 2-
propylthiophane-3,4-trans-dicarboxhydrazide (XIIa) in 5 cc. of 1 N hydrochloric acid and
10 cc. of chloroform was added a t 20" dropwise with stirring a solution of 0.30 g. of sodium
nitrite in 3 cc. of water over a period of five minutes. After being stirred an additional
ten minutes, the chloroform layer was separated and the aqueous layer extracted with
chloroform. The combined extracts were dried with calcium chloride at 0". After dilu-
tion with 10 cc. of absolute ethanol, the solution was refluxed one hour, then evaporated to
dryness. The residue was triturated with carbon tetrachloride; yield, 0.22 g. (37%) of
white crystals, m.p. 170-172". Recrystallization from ethyl acetate did not change the
m.p.
ilnal. Calc'd for C ~ S H * ~ N ~C, O& : H, 7.9;N,9.2.
51.3;
Found: C, 51.5;H, 7.5;N,9.3.
When the diazotization was carried out a t 0" the yield was 30%.
.
2- (y -Ph enox yprop yl) th iophane-3,4-trans-dicarbethoxyaminothiophane (XIIIb) A. From
160 mg. of 2-(~-phenoxypropyl)thiophane-3,4-trans-dicarboxhydrazide was obtained 70 mg.
(37%) of the diurethan, m.p. 172-173"in the same manner as described above for the cor-
responding 2-propyl compound.
dnal. Calc'd for CI~H&:O;S: C, 57.7;H, 7.1;N,7.1.
Found: C , 57.7;H, 6.5;N,7.2.
R. A mixture of 2.8 g. of 2-(y-phenoxypropy1)thiophane-3,4-trans-dicarboxylic acid
(Xlb), 10 cc. of benzene, 5 cc. of thionyl chloride, and 1 cc. of a solution of one drop of
pyridine in 10 cc. of benzene was refluxed for fifteen minutes, gas evolution being complete
in ten minutes. The solution was evaporated in vacuo, the residue dissolved in 20 CC. of
benzene, and the evaporation repeated. A solution of the residue in 20 cc. of acetone was
added dropwise over a period of five minutes t o a solution of 2.8 g. of sodium azide in 20
cc. of water at 15-20'. After being stirred one hour the mixture was diluted with 50 cc. of
water and the oily azide estracted with chloroform. The extracts, dried with calcium
chloride a t OD, were diluted with 25 cc. of absolute ethanol. refluxed thirty minutes, and
evaporated. The crystalline residue was heated to boiling with 15 cc. of absolute ethanol,
cooled to room temperature and the product collected on a filter; yield, 2.1 g. (58%), m.p.
169-170". A mixed m.p. with preparation A was 170-171°.
trans-4-Yethyl-5-(6-phenoxybutyl)-4,6-dihydro-2-imidazolone. A mixture of 200 mg. of
2-(y-phenoxypropyl)-3,4-trans-dicarbethoxyaminothiophane (XIIb), one-half teaspoon of
desulfurizing Raney nickel (IS),and 55 cc. of 75% alcohol was refluxed for thirty minutes.
The nickel was removed by centrifugation and washed with 20 cc. of acetone. The com-
bined solutions were evaporated t o dryness in vacuo. The residue was extracted with ace-
152 BAKER, QUERRY, SBFIR, AND BERNSTEIX
tone, separated from a little inorganic material, and evaporated. The residual colorless
oil did not crystallize. It was refluxed with 0.5 g. of potassium hydroxide and 2 cc. of
methanol for thirty minutes, then diluted with 20 cc. of water. The white crystals had the
m.p. 145-147"; yield, S5 mg. (68%). Recrystallization from 50% alcohol raised the m.p.
to 148-149". The ureide is only slightly soluble in hot acetone and contains no sulfur.
Anal. Calc'd for C1rHd?10: C, 67.7; H, 8.1; N, 11.3.
Found: C, 67.6; H, S.4; N, 11.0.
Recently, Hafmann (19) described the same type of ring closure of a diurethan t o an
imidazolone by mild hydrolysis.
2-Propylthiophane-8,4-cis-dzcarboximide(XXIII). A mixture of 0.50 g. of 2-propyl-
thiophane-3,4-cis-dicarboxylicacid (XIa) and 5 cc. of acetyl chloride was refluxed for
twenty minutes. Evaporation in vacuo gave an oily anhydride. After the addition of 1
cc. of 2S% ammonia water the solution was heated on the steam-bath for thirty minutes,
then at 160" for one hour. The niivture m s cooled and diluted with water; yield 0.35 g.
(77%), m.p. 86-90". Recrystallization from benzene-petroleum ether with the aid of Norit
gave white crystals, m.p. 94-96'.
Anal. Calc'd for CgHl3XO2S:N , 7.0. Found: K,6.9.
A solution of 170 mg. of the cis imide (XXIII) in 0.4 cc. of 85% hydrazine hydrate was
heated on the steam-bath under reflux for fifteen hours. The solid was triturated with
methanol; yield, 110 mg., of 2-propylthiophane-3,4-trans-dicarboxhydrazide, m.p. 2.20'
dec. which was identified by a mixed m.p.
Several attempted Hofmann degradations with aqueous or niethanolic sodium hypo-
bromite gave no crystalline products.
2-Propylthiophane-S,4-czs-dzcarboxy-N, N'-monohydrazide ( X X I V ) . To the anhydride
from 0.50 g. of 2-propylthiophane-3,4-cis-dicarboxylic acid (XIa) prepared as above with
acetyl chloride was added 0.5 cc. of S5% hydrazine hydrate. The solution was dissolved in
20 cc. of water, acidified with 2 cc. of acetic acid, and heated on the steam-bath for fifteen
minutes. The cooled solution was extracted twice with benzene, the extracts Fashed with
aqueous sodium bicarbonate, and concentrated t o 5 cc. Dilution with petroleum ether
gave 0.25 g. (50%) of product. m.p. 76-79". Recrystallization from benzene-petroleum
eLher gave white crystals, m.p. 81-82".
Anal. Calc'd for C9H1*02N2S:K, 13.1. Found: K, 13.2.
The cyclic hydrazide structure (XXIV) was assigned on the basis of solubility in aqueous
alkali and insolubility in 1AT hydrochloric acid or dilute sodium bicarbonste solution.
A mixture of 120 mg. of the cyclic hydrazide (XXIV) and 0.4 cc. of 85% hydrazine hy-
drate was heated on the steam-bath for t n o hours. Trituration with methanol gave white
crystals, m.p. 232" dec., identical with 2-propglthiophane-3,4-trans-dicarboxhydrazide
(XIIa). When the same reaction was carried out in 5 cc. of butanol a t the b.p. as a solvent,
starting material was the only compound which could be isolated.
2-PropyZ-S,4-trans-dia~inothiophanesulfate. To a filtered solution of 3 g. of barium
hydroxide in 15 cc. of water was added 0.52 g. of 2-propyl-3,4-trans-dicarbethoxyaminothio-
phane (XIIIa) in 10 cc. of methanol. After being refluxed for twenty-four hours, the mix-
ture vias just acidified with dilute sulfuric acid, and the filtered solution evaporated to
dryness in vacuo. Trituration with acetone gave 0.28 g. (64%) of white crystals 11-hich were
recrystallized from water. The sulfate gradually decomposes above 300" without melting.
Anal. Calc'd for C ~ H I ~ N ~ OC, Z : H , 7.0; N,10.8; Sod-, 37.2.
~ S32.6;
Found: C, 32 9; H, 6.6; K, 10.8; SO*-, 36.8.
Action of 48% h ydrobTomic acid on 2-(7-phenoxypropyl)-S,Q-trans-dzcarbethoxya~ninothio-
phane (XIIIb). A mixture of 1.7 g . of the urethan and 25 cc. of 48% hydrobromic acid was
refluxed under an air condenser for two honrs, then evaporated to dryness in uacuo. The
residue solidified on trituration with absolute alcohol; yield, 1.4 g . For analysis a sample
of the bromide was dissolved in water and precipitated by the addition of absolute alcohol,
m.p., gradually decomposes over 200".
BIOTIS. I 153
SUMMARY