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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616270생성일: 2026년 10월 25일

Acetic Anhydride → Alpha-acetamido-6-methylindole-3-acrylic acid ethylester

https://huagongshe.com/reaction/616270

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물2-Acetamido-3-ethoxy-3-oxopropanoic acidHCID 3276255—
반응물6-Methylindole-3-carboxaldehydeHCID 4777902—
용매PyridineHCID 1049—
생성물Alpha-acetamido-6-methylindole-3-acrylic acid ethylesterHCID 5417582589%

반응 단계

A 3-l. three-necked flask, equipped with a mechanical stirrer, a thermometer and a dropping funnel with pressure-equalizing arm was charged with 100 g (0.63 mol) of 6-methylindole-3-carboxaldehyde, 119 g (0.63 mol) of acetamidomalonic acid monoethylester and 500 ml of pyridine. The mixture was stirred and kept at 15° with a cold water bath while 175 ml of acetic anhydride was added over 15 minutes. The yellow solution was stirred at room temperature for 3 hours. Then an additional portion of 36 g (0.19 mol) of acetamidomalonic acid monoethyl ester was added and stirring at room temperature was continued for 22 hours before 1 kg of ice was added. The temperature fell to -10° and the product began to precipitate. The suspension was stirred at room temperature for 5 hours and poured into 2 1 of water. After 20 minutes, the precipitate was collected by suction filtration, washed with water and dried at 50° in an air oven overnight to afford 159.5 g (89%) of crude product as yellow crystals, m.p. 159°-162° (sinters at 75°).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04073795
출처 데이터셋uspto-grants-1978_02
ORD IDord-e133900a9c3641189a1bfb2f1c91b88c
출처 메모uspto-grants-1978_02