돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 461545생성일: 2026년 10월 25일

Ethyl bromoacetate → 3-Benzoyloxy-6,7-dimethoxy-9-carbethoxymethyl-1,2,3,4-tetrahydrocarbazole

https://huagongshe.com/reaction/461545

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Sodium hydrideHCID 24758—
반응물3-Benzoyloxy-6,7-dimethoxy-1,2,3,4-tetrahydrocarbazoleHCID 12891777—
용매DimethylformamideHCID 6228—
생성물3-Benzoyloxy-6,7-dimethoxy-9-carbethoxymethyl-1,2,3,4-tetrahydrocarbazoleHCID 12891850—

반응 단계

The 3-benzoyloxy-6,7-dimethoxy-9-carbethoxymethyl-1,2,3,4-tetrahydrocarbazole was prepared by following an alkylation procedure similar to that described in Example 11 but using 17.6 g. of 3-benzoyloxy-6,7-dimethoxy-1,2,3,4-tetrahydrocarbazole (see Example 4) and 2.14 g. of sodium hydride (56% in mineral oil) in 200 ml. of dimethylformamide, and 8.4 g. of ethyl bromoacetate. The crude product in ethyl acetate was filtered through alumina, the filtrate was evaporated to dryness under reduced pressure and the residue was recrystallized from ethyl acetate to give 3-benzoyloxy-6,7-dimethoxy-9-carbethoxymethyl-1,2,3,4-tetrahydrocarbazole, m.p. 125°-127° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04062864
출처 데이터셋uspto-grants-1977_12
ORD IDord-34dfc5cdba8a42b0a8aa852790f7ddf3
출처 메모uspto-grants-1977_12