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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248494생성일: 2026년 10월 25일

Benzenesulfonyl chloride → 1H-Indole, 3-acetyl-1-(phenylsulfonyl)-

https://huagongshe.com/reaction/248494

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물3-AcetylindoleHCID 12802—
반응물Potassium HydroxideHCID 14797—
반응물Ammonium ChlorideHCID 25517—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물1H-Indole, 3-acetyl-1-(phenylsulfonyl)-HCID 848535—

반응 조건

온도0 °C

반응 단계

To a solution of 41.39 g of 3-acetyl indole in 300 ml of dimethyl sulfoxide at 0° C. was added a solution of 18.6 g of potassium hydroxide in 20 ml of water. This mixture was stirred at 0° C. for 2 hours, then 47.6 ml of benzenesulfonyl chloride was added dropwise over 40 minutes. The mixture was stirred for an additional 30 mInutes, then poured into aqueous ammonium chloride and extracted several times with ether. The ether extracts were combined, washed with water, dried and evaporated, giving 59.8 g of 3-acetyl-N-phenylsulfonyl indole.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210193
출처 데이터셋uspto-grants-1993_05
ORD IDord-3dcfc7d0edb84b4c8073d9f8123bacf1
출처 메모uspto-grants-1993_05