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One-Pot Preparation of Phenylpropanoid Esters
One-Pot Preparation of Phenylpropanoid Esters
DOI 10.1007/s11164-011-0338-3
Zhen-Hua Jiang
Received: 30 March 2011 / Accepted: 7 June 2011 / Published online: 23 June 2011
Ó Springer Science+Business Media B.V. 2011
Introduction
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208 H. Wang et al.
are common constituents of plant tissues. Apart from their antioxidant capacity, these
cinnamates, bearing hydroxyl and/or methoxyl groups, present several biological and
pharmacological properties such as antimicrobial, anti-carcinogenic, antifungal, anti-
aging, and anti-atherosclerosis effects [1–8]. Furthermore, hydrocinnamate is a key
precursor of 1,3,4,9-tetrahydropyrano [3,4-b] indole-1-acetic acid, which is used as
an analgesic, inflammation inhibitor, and antipyretic [9]. Hydrocinnamate has also
been used for the synthesis of HIV-1 protease inhibitors [10]. P-methoxycinnamates
are commercially popular UV-B screening compounds in sunscreen products [11].
Particularly, cinnamates have a wide range of industrial applications such as
plasticizers, graphics, lubricants, flavors, perfumes, and cosmetics [12]. Due to their
distinguished properties and applications of phenylpropanoid esters, there has been
great interest in devising simple and efficient methods to prepare them.
The typical methods for synthesis of phenylpropanoid esters are the direct
esterification methods of substituted cinnamic acid catalyzed by chemicals.
However, most of the procedures require strong acids such as sulfuric acid,
hydrochloride acid, and toxic chemicals such as dimethyl sulfate, methyl iodide, or
diazomethane, which are environmentally hazardous and hence unacceptable.
Enzyme-catalyzed esterification ways have the reputation of green, but these
methods often suffer from unsatisfactory yields and expensive raw material [13–19].
Knoevenagel condensation between substituted benzaldehyde and monomalonate is
a useful alternative to the esterification method. Monomalonate can usually be
prepared by the reaction of alcohols and Meldrum’s acid [20]. Monomalonate can
also be synthesized by the monoesterification of malonic acid catalyzed by boric
acid [21]. Inspired by this method for monomalonate, we successfully developed a
general, efficient, and convenient process for the synthesis of phenylpropanoid
esters from malonic acid, alcohols, and corresponding benzaldehydes in one-pot in
the presence of boric acid and piperidine. Briefly, the alcohols reacted with malonic
acid to form monomalonates, which without separation, immediately reacted with
aldehydes in the presence of piperidine to afford the title compounds (Scheme 1).
R3
O
R2 CHO
CO2H H3BO3 OR1
R1OH +
CO2H piperidine
CO2H
without separation
R3 O
R2 OR1
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One-pot preparation of phenylpropanoid esters 209
The reactions involved the one-pot condensation of malonic acid, alcohols, and
aldehydes in the presence of a catalytic amount of boric acid and pyridine to afford
phenylpropanoid esters in moderate to excellent yield (70–86%). The ratio of
malonic acid, alcohol, aldehyde, boric acid, and piperidine was in a molar ratio of
1:1:0.7:0.1:0.3. First, the influence of the adding order of reagents on the yields was
investigated. Procedure 2 (entry 2 in Table 1): first let the reaction between
benzaldehyde, cinnamic acid, ethanol, and boric acid take place in toluene for 18 h.
Piperidine was then injected and the reaction was continued for another 12 h. The
conversion of aldehyde was evaluated by GC and the yields of product refer to the
isolated ones. The yield by procedure 2 is about 72.1%. Procedure 3 (entry 3 in
Table 1) is by treatment of benzaldehyde, cinnamic acid, ethanol, boric acid, and
piperidine all together in toluene for 30 h, then the conversation of aldehyde and the
isolated yield was evaluated. The yield by procedure 3 was about 50.3%. This
indicates that the adding order of raw material had great effects on the yields when
the conversation of aldehyde was almost the same (above 99%). Procedure 1 is the
best working one among the three procedures (entry 1 in Table 1), in which
monomalonate was first produced by the reaction of malonic acid and alcohol
catalyzed by boric acid. Then Knoevenagel condensation of monomalonate was
carried out by injection of aldehyde and piperidine leading to the formation of ethyl
cinnamate in 84.7% yield. Therefore, in the following synthesis of the target
products, procedure 1 was adopted as the typical method. The possible reaction
mechanism is as follows: First monomalonates were produced by the reaction of
cinnamic acid and alcohols catalyzed by boric acid [21], then monomalonates
reacted with aldehydes, leading to Knoevenagel condensation products catalyzed by
piperidine. Finally, the condensed products were decarboxylated under the heating
condition and the presence of catalysts gave the title compounds.
In order to explore the scope and limitations of this synthetic methodology, we
have extended this procedure for different alcohols and benzaldehydes bearing
hydroxyl and/or methoxyl groups, which the corresponding esters often possess
various medicinal functions. The desired esters were obtained and are listed in
Table 2. Table 2 shows that lower isolated yields were obtained for aromatic
aldehydes bearing electron-donating groups on the benzene ring, which may be
ascribed to the lower electropositivity of the carbonyl. The electron-donating effects
intrinsically deactivate the electrophilic carbon center of the aldehyde group for
nucleophilic attack of the enolate anion of monomalonate. The yields of the esters
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210 H. Wang et al.
1 Me H H 30 86.3
2 Et H H 30 84.7
3 Isopropyl H H 30 78.2
4 Me OH H 35 78.3
5 Et OH H 35 76.1
6 Isopropyl OH H 35 70.6
7 Me OMe H 35 83.9
8 Et OMe H 35 79.5
9 Isopropyl OMe H 35 75.2
10 Me OH OMe 35 76.9
11 Et OH OMe 35 74.3
12 Isopropyl OH OMe 35 70.1
Conclusions
In summary, boric acid and piperidine was shown to be an effective and cheap
co-catalyst for the preparation of phenylpropanoid esters derivatives. The one-pot
process offers several unique advantages such as enhanced yields, economic raw
material, operational simplicity, and mild reaction conditions.
Experimental section
All the substituted aldehydes, malonic acid, and other chemicals were purchased
from Shanghai Reagent Co. The 1H NMR spectra were obtained with a DPX
600 MHz spectrometer in CDCl3 with TMS as internal standard. The IR spectra
were recorded on an Avatar 330 instrument as potassium bromide pellets. The MS
spectra were performed by using an Agilent 5975c mass spectrometer in the EI
mode. Yields refer to isolated products.
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One-pot preparation of phenylpropanoid esters 211
Malonic acid (1.001 g, 9.62 mmol), and boric acid (0.059 g, 0.96 mmol) were
added to the ethanol (0.56 mL, 9.62 mmol) in a two-necked round-bottomed flask
with a drying tube. After refluxing for about 18 h, benzaldehyde (0.72 g,
6.73 mmol), piperidine (0.3 mL, 2.89 mmol) and toluene (5 mL) were added into
the mixture with stirring. When the reaction was finished by TLC monitoring,
solvents were removed by distillation under vacuum. The residue was dissolved in
ethyl acetate (about 30 mL), then washed with saturated solutions of sodium
bicarbonate(20 mL 9 2), sodium bisulfite (20 mL 9 2), distilled water (20 mL),
respectively. The organic phase was dried by anhydrous MgSO4 overnight. After
removal of the solvent, the crude product was given. Pure product was produced by
silica gel column chromatography.
Methyl cinnamate (1), Pale yellow solid, mp 31–32 °C, IR (KBr, cm-1), 1,717
(C=O), 1,638 (C=C), 1,272, 1,173 (C–O–C), 1H NMR (600 MHz, CDCl3, d ppm),
7.670–7.644 (1H, d, J = 15.6 Hz, =CH), 7.479–7.454 (2H, m, ArH), 7.378–7.318
(3H, m, ArH), 6.390–6.363 (1H, d, J = 16.2 Hz, =CH), 3.740 (3H, s, OCH3). MS
(m/z, %), 162 (M?, 60%), 131 (100%), 103 (70%), 77 (45%).
Ethyl cinnamate (2), colorless oil, IR (KBr, cm-1), 1713 (C=O), 1,637 (C=C),
1,268, 1,173 (C–O–C), 1H NMR (600 MHz, CDCl3, d ppm), d 7.635–7.609 (1H, d,
J = 15.6 Hz, =CH), 7.491–7.412 (2H, m, ArH), 7.363–7.315 (3H, m, ArH),
6.387–6.361 (1H, d, J=15.6 Hz, =CH), 4.237–4.196 (2H, q, J = 7.8 Hz, CH2),
1.285–1.263 (3H, t, J = 6.6 Hz, CH3), MS (m/z, %), 176 (M?, 40%), 131 (100%),
103 (50%), 77 (40%).
Isopropyl cinnamate (3), colorless oil, IR (KBr, cm-1), 1,712 (C=O), 1,637
(C=C), 1,180, 1,108 (C–O–C), 1H NMR (600 MHz, CDCl3, d ppm), d 7.614–7.587
(1H, d, J = 16.2 Hz, =CH), 7.463–7.430 (2H, m, ArH), 7.331–7.306 (3H, m, ArH),
6.367–6.340 (1H, d, J = 16.2 Hz, =CH), 5.106–5.044 (1H, m, CH), 1.254–1.243
(6H, d, J = 6.6 Hz, (CH3)2), MS (m/z, %), 190 (M?, 30%), 147 (80%), 131 (100%),
103 (50%), 77 (40%).
Methyl p-hydroxycinnamate (4), white solid, mp 129–130 °C, IR (KBr, cm-1),
3,378 (O–H), 1,686 (C=O), 1,633 (C=C), 1,197, 1,170 (C–O–C), 1H NMR
(600 MHz, CDCl3, d ppm), d 7.588–7.561 (1H, d, J = 16.2 Hz, =CH), 6.363–6.349
(2H, d, J = 8.4 Hz, ArH), 6.799–6.784 (2H, d, J = 9.0 Hz, ArH), 6.246–6.219 (1H,
d, J = 16.2 Hz, =CH), 5.927 (1H, s, OH), 3.735 (3H, s, CH3), MS (m/z): 178 (M?,
75%), 147 (100%), 119 (40%).
Ethyl p-hydroxycinnamate (5), white solid, mp 70–71 °C, IR (KBr, cm-1), 3,286
(O–H), 1,683 (C=O), 1,632 (C=C), 1,190, 1,168 (C–O–C), 1H NMR (600 MHz,
CDCl3, d ppm), 7.578–7.551 (1H, d, J = 16.2 Hz, =CH), 7.361–7.346 (2H, d,
J = 9.0 Hz, ArH), 6.795–6.781 (2H, d, J = 8.4 Hz, ArH), 6.241–6.215 (1H, d,
J = 15.6 Hz, =CH), 5.96 (1H, s, OH), 4.211–4.175 (2H, q, J = 7.2 Hz, CH2),
1.279–1.255 (3H, t, J = 7.2 Hz, CH3), MS (m/z): 192 (M?, 50%), 147 (100%).
Isopropyl p-hydroxycinnamate (6), pale yellow solid, mp 80–81 °C, IR (KBr,
cm-1), 3,357 (O–H), 1,679 (C = O), 1,632 (C=C), 1,203, 1,170 (C–O–C), 1H NMR
(600 MHz, CDCl3, d ppm), 7.557–7.530 (1H, d, J = 16.2 Hz, = CH), 7.351–7.337
(2H, d, J = 8.4 Hz, ArH), 6.784–6.770 (2H, d, J = 8.4 Hz, ArH), 6.222–6.195
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212 H. Wang et al.
(1H, d, J = 16.2 Hz, =CH), 5.952 (1H, s, OH), 5.089–5.047 (1H, m, CH),
1.248–1.237 (6H, d, J = 6.6 Hz, (CH3)2), MS (m/z, %):206 (M?, 45%), 164 (50%),
147 (100%).
Methyl p-methoxycinnamate (7), pale yellow solid, mp 88–89 °C, IR (KBr,
cm-1), 1,717 (C=O), 1,637 (C=C), 1,206, 1,170 (C–O–C), 1H NMR (600 MHz,
CDCl3, d ppm), 7.596–7.570 (1H, d, J = 15.6 Hz, =CH), 7.415–7.401 (2H, d,
J = 8.4 Hz, ArH), 6.843–6.829(2H, d, J = 8.4 Hz, ArH), 6.256–6.230 (1H, d,
J = 15.6 Hz, = CH), 3.769 (3H, s, OCH3), 3.724 (3H, s, OCH3), MS (m/z, %):192
(M?, 100%), 161 (90%), 133 (25%).
Ethyl p-methoxycinnamate (8), pale yellow oil, IR (KBr, cm-1), 1,709 (C=O),
1,633 (C=C), 1,205, 1,173 (C–O–C), 1H NMR (600 MHz, CDCl3, d ppm),
7.572–7.546(1H, d, J = 15.6 Hz, =CH), 7.409–7.398 (2H, d, J = 6.6 Hz, ArH),
6.835–6.824 (2H, d, J = 6.6 Hz, ArH), 6.238–6.211 (1H, d, J = 16.2 MHz, =CH),
4.187–4.152 (2H, q, J = 6.9 Hz, CH2), 3.749 (3H, s, OCH3), 1.260–1.237 (3H, t,
J = 6.9 Hz, CH3), MS (m/z, %), 206 (M?, 100%), 161 (70%), 134 (20%).
Isopropyl p-methoxycinnamate (9), yellow oil IR (KBr, cm-1), 1,706 (C=O),
1,634 (C=C), 1,204, 1,172 (C–O–C), 1H NMR (600 MHz, CDCl3, d ppm),
7.565–7.539 (1H, d, J = 15.6 Hz, =CH), 7.410–7.3969 (2H, d, J = 8.4 Hz, ArH),
6.836–6.822 (2H, d, J = 8.4 Hz, ArH), 6.232–6.205 (1H, d, J = 16.2 Hz, =CH),
5.080–5.039 (1H, m, CH), 3.765 (3H, s, OCH3), 1.241–1.231 (6H, d, J = 6.0 Hz,
(CH3)2), MS (m/z,%), 220 (M?, 100%), 161 (40%), 134 (60%).
Methyl ferulate (10), white solid, mp, 64–65 °C, IR (KBr, cm-1), 3,407 (O–H),
1,703 (C=O), 1,633 (C=C), 1,269, 1,167 (C–O–C), 1H NMR (600 MHz, CDCl3, d
ppm), 7.557–7.531 (1H, d, J = 15.6 Hz, =CH), 7.024–6.948 (2H, m, ArH),
6.859–6.848 (1H, d, J = 6.6 Hz, ArH), 6.252–6.227 (1H, d, J = 15 Hz, =CH),
5.853 (1H, s, OH), 3.870 (3H, s, OCH3), 3.719 (3H, s, OCH3), MS (m/z, %), 208
(M?, 100%), 177 (75%).
Ethyl ferulate, pale yellow solid, mp, 59–60 °C, IR (KBr, cm-1), 3,411 (O–H),
1,700 (C=O), 1,631 (C=C), 1,265, 1,163 (C–O–C), 1H NMR (600 MHz, CDCl3, d
ppm), 7.558–7.532 (1H, d, J = 15.6 Hz, =CH), 7.027–6.962 (2H, m, ArH),
6.854–6.841 (1H, d, J = 7,8 Hz, ArH), 6.234–6.208 (1H, d, J = 15.6 Hz, =CH),
5.835 (1H, s, OH), 4.204–4.170 (2H, q, J = 6.9 Hz, CH2), 3.854 (3H, s, OCH3),
1.277–1.254 (3H, t, J = 6.9 Hz, CH3), MS (m/z, %), 222 (M?, 100%), 177 (50%),
150 (25%).
Isopropyl ferulate, white solid, mp, 79–80 °C, IR (KBr, cm-1), 3,391 (O–H),
1,691 (C=O), 1,628 (C=C), 1,184, 1,096 (C–O–C), 1H NM (600 MHz, CDCl3, d
ppm), 7.538–7.511 (1H, d, J = 16.2 Hz, =CH), 7.029–6.961 (2H, m, ArH),
6.850–6.836 (1H, d, J = 8.4 Hz, ArH), 6.215–6.189 (1H, d, J = 15.6 Hz, =CH),
5.827 (1H, s, OH), 5.085–5.044 (1H, m, CH), 3.850 (3H, s, OCH3), 1.244–1.234
(6H, d, J = 6.0 Hz, (CH3)2), MS (m/z, %), 236 (M?, 100%), 177 (25%), 150
(20%).
Acknowledgments This study was supported by the National Natural Science Foundation of China
(Grant no. 20702016).
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One-pot preparation of phenylpropanoid esters 213
References
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