Organic Syntheses, Coll. Vol. 2, p.612 (1943); Vol. 10, p.100 (1930).
.—In an 8-l. (2-gal.) bottle
is placed 600 g. of commercial casein (coarse powder), which is then covered with about 3.2 l. of tap water at 37° (Note 1)
. The bottle is shaken until all the casein is moistened. A solution of 60 g. of anhydrous sodium carbonate (Note 2)
and 6 g. of sodium fluoride (Note 3)
in 1 l. of water at 37° is added. A thin paste of 20 g. of commercial pancreatin in 100 cc. of water (37°) is poured in. The mixture is covered with a layer of toluene (80 cc.), diluted to 6 l.
, stoppered, shaken thoroughly, and placed in a warm room or bath at 37°.
After four or five days, with daily shakings, most of the casein is in solution and chalky masses of tyrosine
begin to separate. After five days, a second 20-g. portion of pancreatin in 100 cc. of water is added. After twelve days, the bottle is cooled in an icebox
overnight and the undissolved material is filtered (Note 4)
and reserved for the preparation of tyrosine
The filtrate (6.9–7 l.) is measured into a 16-l. (4-gal.) stone jar
, and for every liter there is added 163 cc. of dilute sulfuric acid
(one volume of 95 per cent sulfuric acid
and one volume of water, cooled to room temperature). The first part of the acid must be added cautiously on account of the liberation of carbon dioxide
is precipitated by adding a solution of 200 g. of mercuric sulfate (Note 5)
in a mixture of 1860 cc. of water and 140 cc. of 95 per cent sulfuric acid
. After standing for twenty-four to forty-eight hours, the clear liquid is siphoned out and the yellow precipitate is filtered and washed (Note 6)
with a solution of 100 cc. of concentrated sulfuric acid
in 1.9 l. of distilled water containing 20 g. of mercuric sulfate
, until the filtrate is colorless and Millon's test is atypical (Note 7)
; about 1.5 l. is necessary. The precipitate is washed with three successive 500-cc. portions of distilled water to remove most of the sulfuric acid
The moist precipitate (120–130 g.) is suspended with mechanical stirring in 1.2–1.3 l. of distilled water, and a hot, 20 per cent aqueous solution of barium hydroxide
is added until the mixture is permanently alkaline to phenolphthalein (about 120 cc. is required)
. A rapid stream of hydrogen sulfide
is passed in with stirring until the mercury
is completely precipitated (Note 8)
. The precipitate is filtered and washed with water until a sample of the washings gives a negative test for tryptophane
with bromine water (Note 9)
. The barium
is removed from the combined filtrate and washings by adding the exact amount of dilute sulfuric acid (Note 10)
and filtering. The filtrate is concentrated under reduced pressure to about 80 cc.
is extracted from the aqueous solution by repeated shaking in a separatory funnel
with 25-cc. quantities of n-butyl alcohol
; water is added from time to time to keep the volume approximately constant (Note 11)
. The butyl alcohol
extract is distilled under reduced pressure. After the water present has distilled, the tryptophane
precipitates in the distilling flask and may cause bumping. When all the water has been removed, as is indicated by non-formation of drops on the side of the condenser, the distillation is stopped and, after cooling, the tryptophane
is filtered and washed with a little fresh butyl alcohol
. Such extractions and distillations are continued until the quantities of tryptophane
obtained are negligibly small (Note 11)
so produced (7–8 g.) varies somewhat in quality in different runs. It is purified by recrystallization from 60 cc. of dilute alcohol (two volumes of 95 per cent alcohol to one volume of water)
, filtering from the hot solution an appreciable quantity of insoluble matter, and subjecting this to a second extraction with an additional 10 cc. of aqueous alcohol
. The solution is decolorized by the addition of 1 g. of Norite
and allowed to stand in the icebox; the silvery leaflets of tryptophane
are filtered and washed successively with cold 70 per cent, 80 per cent, 95 per cent alcohol
, and, finally, with a little ether
. Less than half the tryptophane
is obtained in each crystallization (Note 12)
. The yield of pure (Note 13) tryptophane
is 4.0–4.1 g.
, together with under 0.1 g. of less pure product.
.—The insoluble material (160–170 g.) obtained on filtering the digestion mixture (p. 612)
is suspended in 320 cc. of water and 80 cc. of 36 per cent hydrochloric acid
, and the mixture is boiled gently for thirty minutes (Note 14)
. After straining through cheesecloth, decolorizing with 6 g. of Norite (Note 15)
, and filtering hot (Note 16)
, the warm (60–70°) solution is shaken with three 20-cc. portions of benzene (Note 17)
and heated to boiling (Note 18)
. A slight excess (120–150 cc.) of 28 per cent ammonia
is cautiously added, and the mixture is allowed to stand overnight in the icebox. The crystalline product is then filtered and washed with three 40-cc. portions of ice-water. After drying, it weighs about 23 g. The mother liquor and washings are evaporated to about 200 cc., when a second crop is obtained, weighing slightly under 1 g.
The combined product is suspended in 400 cc. of water and dissolved by adding 8 g. of sodium hydroxide
in 20–30 cc. of water (Note 19)
; 2 g. of Norite
is added, and the solution filtered. The residue is washed on the funnel with 20–30 cc. of hot distilled water. The filtrate is heated to boiling (Note 18)
and treated with 13 cc. of hydrochloric acid (Note 20)
, when crystallization usually begins. The mixture is then acidified to litmus with acetic acid (Note 21)
and allowed to stand overnight in the refrigerator. The resulting tyrosine
is filtered and washed with ice-cold distilled water (130–150 cc. is necessary) until the washings are free of chloride. The product is dried in air or in a vacuum oven. The yield is 17.0–18.2 g.
of pure white, silky needles of tyrosine
. A second crop (about 0.5 g.) of a slightly less pure product may be obtained on concentrating the mother liquor to about 120 cc.
Tryptic action is more rapid if all water used is at 37°. Distilled water is not necessary at this stage.
This is a considerable excess of sodium carbonate
. Smaller quantities might be satisfactory.
This filtration may be slow. Büchner funnels of 20-cm. diameter
are best used; the material from a single filling is allowed to suck dry and the filter paper
A persistent red color is always obtained in the filtrates, but the final color is distinctly different from that due to tyrosine
This amount is best determined in a 20-cc. aliquot sample, employing 2 per cent sulfuric acid
in a buret
In checking, it was found satisfactory to extract in a continuous apparatus (Fig. 21)
. Extraction is continued until the liquid in the flask begins to bump on account of the separation of solid; a new charge of butyl alcohol
is then employed, about five charges being necessary. This process is repeated until the residue after a three-hour period of extraction fails to give the red color, characteristic of tryptophane
, with bromine water
. The time necessary, of course, depends upon the rate of boiling; in checking, it was found to be twenty-eight to thirty hours.
The recrystallization of the crude tryptophane
is an extremely troublesome process. Not only must a less soluble by-product be removed, but the mother liquors contain a more soluble, gummy impurity in considerable proportion. After collecting each crop, the mother liquor must be evaporated to a small volume on the steam bath
and treated with a double volume of alcohol. This process is repeated until no further crystals are obtained, but only a gum.
The purity of the tryptophane
has been checked by the optical rotation ([α]D = −28 to −33°
) and by analysis for amino nitrogen (6.8–6.9 per cent) by Van Slyke's method.
The boiling acid solution hydrolyzes protein material that otherwise greatly retards filtration.
used in this preparation is insufficient to decolorize the solutions completely but gives a white final product.
All the filtrations in the purification of tyrosine
, except possibly the last, are best done on a 20-cm. Büchner funnel
. Whenever charcoal is used, kieselguhr may be employed to obtain a clear filtrate.
extracts traces of substances, probably fatty acid, that retard filtration and greatly alter the quality of the final product.
crystallizes in long, silky needles, easy to filter, if the solution is neutralized at the boiling point.
A small amount of flocculent impurity remains undissolved.
The hydrochloric acid
is added to provide chloride ion as an index of complete washing.
Copyright © 1921-, Organic Syntheses, Inc. All Rights Reserved