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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616265생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/616265

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-l. 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 alphanitro-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 12N 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-9N 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 번호US04073795
출처 데이터셋uspto-grants-1978_02
ORD IDord-a8cd8684b403480a844901a782c1c76b
출처 메모uspto-grants-1978_02