돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2270969생성일: 2026년 10월 25일

Acetic Anhydride → 3-Acetyl-1-benzenesulfonylindole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/2270969

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물1H-Indole-5-carboxylic acid, 1-(phenylsulfonyl)-, methyl esterHCID 57517433—
용매1,1-DichloroethaneHCID 6365—
생성물3-Acetyl-1-benzenesulfonylindole-5-carboxylic acid methyl esterHCID 6989028096%

반응 단계

To a suspension of 10.7 g (80 mmol) of aluminum chloride in dichloroethane (80 ml) was added dropwise 4.83 g (40 mmol) of acetic anhydride. After stirring for 15 min, to the mixture was added dropwise 6.31 g (20 mmol) of the above-mentioned 1-benzenesulfonylindole-5-carboxylic acid methyl ester in dichloroethane (60 ml). After stirring for 2 hours at room temperature, to the mixture were added 5.33 g (40 mmol) of aluminum chloride and 2.04 g (20 mmol) of acetic anhydride. After stirring for 30 min, the mixture was poured into ice-water, extracted with ethyl acetate. The extract was washed twice with water, aqueous sodium bicarbonate and dried, and then concentrated. The obtained crystal was washed with isopropyl ether to give 6.82 g of 3-acetyl-1-benzenesulfonylindole-5-carboxylic acid methyl ester. Yield: 96%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06333323B1
출처 데이터셋uspto-grants-2001_12
ORD IDord-7988fd239167492c82cfcab229980e81
출처 메모uspto-grants-2001_12