Chloroacetic Acid → S-(Carboxymethyl)cysteine

HRID 1649338

반응식

HRID 1649338 반응식
Cl.[NH2:2][CH:3]([C:6]([OH:8])=[O:7])[CH2:4][SH:5].[OH-].[Na+].S.[Na].Cl[CH2:14][C:15]([OH:17])=[O:16]>O>[C:15]([CH2:14][S:5][CH2:4][CH:3]([C:6]([OH:8])=[O:7])[NH2:2])([OH:17])=[O:16]

참가 물질

6

실험 절차

As starting material, there served (RS)-cysteine hydrochloride which was produced by the process of German OS No. 2645748. 140 grams (1 mole) of this material together with 160 grams (4 moles) of sodium hydroxide were dissolved in 1000 ml of water. To this solution there was first added 3 grams of sodium hydrogen sulfide and then in the course of 45 minutes 95 grams (1 mole) of monochloroacetic acid. The temperature of the mixture in the meanwhile was held at 20° C., and after that held for 3 hours at 20° to 30° C., the reaction mixture was subsequently adjusted to a pH of 3.0 by addition of concentrated, aqueous hydrochloric acid. Hereby, the S-(carboxymethyl)-(RS)-cysteine separated out. It was filtered off at 10° C., and washed with water until it was free from chloride ions. Then, it was dried under reduced pressure at 105° C. The yield was 173 grams, corresponding to 97% based on the cysteine hydrochloride employed. The melting point (decomposition point) of the S-(carboxymethyl)-(RS)-cysteine was 188° to 192° C.

후처리

  1. customwas produced by the process of German OS No
  2. customwas held at 20° C.
  3. additionthe reaction mixture was subsequently adjusted to a pH of 3.0 by addition
  4. concentrationof concentrated
  5. customHereby, the S-(carboxymethyl)-(RS)-cysteine separated out
  6. filtrationIt was filtered off at 10° C.
  7. washwashed with water until it
  8. customThen, it was dried under reduced pressure at 105° C
  9. customwas 188° to 192° C.

출처 및 근거

ORD 기록
ord-77944b1c3be64677ae9555f3b00915b3
출처 데이터셋
uspto-grants-1983_11
특허 번호
US04416828

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