1. The document describes a process for manufacturing the alkaloid Yohimbine from Yohimbehe bark.
2. The process involves extracting pulverized bark with dilute acetic acid, precipitating the alkaloid with carbonate of soda, and purifying it by recrystallization from alcohol.
3. The alkaloid Yohimbine crystallizes in white needles from alcohol with a melting point of 234 degrees Centigrade and the chemical formula C22H30N2O.
1. The document describes a process for manufacturing the alkaloid Yohimbine from Yohimbehe bark.
2. The process involves extracting pulverized bark with dilute acetic acid, precipitating the alkaloid with carbonate of soda, and purifying it by recrystallization from alcohol.
3. The alkaloid Yohimbine crystallizes in white needles from alcohol with a melting point of 234 degrees Centigrade and the chemical formula C22H30N2O.
1. The document describes a process for manufacturing the alkaloid Yohimbine from Yohimbehe bark.
2. The process involves extracting pulverized bark with dilute acetic acid, precipitating the alkaloid with carbonate of soda, and purifying it by recrystallization from alcohol.
3. The alkaloid Yohimbine crystallizes in white needles from alcohol with a melting point of 234 degrees Centigrade and the chemical formula C22H30N2O.
Date') of Application, 27th June, 1900-Accepted, 11th Aug., 1900
COMPLETE SPECIFICATION.
_Process of Manufacturing Yohimbine.
I, Dr. LEOPOLD SPIEGEL, of No. 21,:, Chausseestrass~, N., Berlin, G'erm.an.y, Chemist, do hereby declare the nature 0£ this invention and in what manner the same is to be performed, to be particularly described and ascertained in and by the ·following stat~ment: - 5 Yohimbine is the active alkaloid o:f yohim.behe bark, which forms an article of export of Kamerun, South-West Africa. The bark is that of a tree belonging to the family: apocynaceae, species. Tubernaemontana. To produce this alkaloid in its pure state the pulverised bark is extracted with dilute acetic acid. From this solution the alkaloid is precipitated by the 10 addition .o:f ca1·bonate of soda, and after drying is purified by recrystallization from alcohol. ·· · Yohimbi0:e corresponds to the formula C22H 30N 0~ or Cs:JHS'dN1p"' it crystal- lizes in the form of white needles melting at 2a4 Jeg1·ees Centigrade. . Its corresponding salts are formed by treating the alkaloid with dilute acids 15 or aqueous solutions of the same and evaporating the solvent until crystalliza- tion 1:iegins. l'he hydrochloric acid salt has the formula 0 22~N1s08 HC1. or . C~30N 1p 8HC1 ; it consists of minute white needl~s, melting at 300 degrees Centigrade. r Yohimbine is easily soluble in methyl-ethyl-, andi amyl-alcohol, ether, ace- ~O tone, and chloroform, less 'soluble.in ben~ol, neady insoluble in water. Its characteristic reactions are the following : It dissolves colourless in con- centrated sulphuric acid, a minute crystal of potassium bichromate added to it produces a zone with a rioh blue-violet margin which slowly turns to a. dull green. 25 With concentrated nitric acid it · forms a colourless solution. which quickly turns a. deep yellow, t.urning a beautiful orange-red on adding an excess of_ caustio soda solution. , Erdmann's reagent causes a dark blue-bJ.ack colour, which · quickly turns greenish and finally yellowish-brown. . _ 30 Having now pa:rticularly described and ascertained. the nature of my said invention and in what manner the sa.me is to be performed I declare t-hat what I claim :is:- · 1. The process of extracting Y ohimbine :from Yohimbehe bark which con- sists in extracting the :pulvedzed bark with dilute acetic acid, precipitating :-rn the alkaloid · with carbonate of soda and purifying the same by recrystallization £rom alcohol. · . 2. Treating Yohimbehe bark with dilute acetic acid substantially as described. 3. Precipitating Yohimbine from an- acetic acid solution by the addition of -carbonate of soda substantially as desciibed. . 40 4. As a new· product of manufacture the alkaloid Yohimbine, crystallizing in white needles from alcohol, near~y insoluble in water, having a melting point .[Prfoe BdJ 'f>~t\MINGH,<4, FREE ~ . _. 2 N° 11,64:7.-A.D. 1000. Spiegel's Process of Manlufa.cturing Yohimb(ne. of 234 degrees Centigrade, and p«;>rrespondin,g to the formula C22H 30N 2 0 i or C~32 N 2 0 41 s-q.bstantially as described. 5. The corr~ponding salts and derivatives which may be pro_d ucod from Yohimbine substantially as d:escriped. . · Dated this 8th day of J u~e 1900. - 5 . ' DR. LEOPOLD SPIEGEL. • . • . ·, _-.;..-.:..:'··-=--•_:_'_,_,_,____:_:__ _' - - ' - - - - - - - - - - - - - Redhill: hi~ted for Iler Maje~ty's Stationery Office. by Malcomson & Co •• Ltd. (G. 557f>-125-ll/1900