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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127499생성일: 2026년 10월 27일

Hydrochloric Acid → Alpha-amino-6-chloro-3-indoleacrylic acid methylester hydrochloride

https://huagongshe.com/reaction/127499

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물MethanolHCID 887—
반응물Alphanitro-6-chloro-3-indoleacrylic acid methylesterHCID 53746644—
용매Diethyl EtherHCID 3283—
생성물Alpha-amino-6-chloro-3-indoleacrylic acid methylester hydrochlorideHCID 70550909180.1%

반응 단계

A 3-1. three-necked flask, equipped with a thermometer and a mechanical stirrer was charged with 316 g (1.4 moles) of stannous chloride dihydrate and a solution of 111 g (3 moles) of dry hydrogen chloride gas in 1 l. of methyl alcohol. The colorless solution was stirred and cooled to -30° in a dry ice-acetone bath. 112.3 g (0.40 moles) of alpha-nitro-6-chloro-3-indoleacrylic acid methylester was added in 4 equal portions over 1 hour, maintaining the temperature between -25° and -20°. After the addition was complete, the temperature was allowed to rise to -10° and stirring at this temperature was continued for 90 minutes. Then 500 ml. of ether was added to the yellow suspension, followed by addition of 500 ml of 12 N hydrochloric acid (concentrated), the temperature was kept below 5°. The mixture was then filtered through a Buchner funnel. The filter cake was washed with 1000 ml of methyl alcohol-9 N aqueous hydrochloric acid 1:1, precooled to -20°, and 400 ml of ether. The tan product was dried at 40°/0.1 mmHg for 8 hours and then at 20°/0.1 mmHg to constant weight to yield 103.4 g (90%) of crude product, m.p. 191° (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04256641
출처 데이터셋uspto-grants-1981_03
ORD IDord-a0e4707512d94dd9990a5c981d0f41ff
출처 메모uspto-grants-1981_03