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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551037생성일: 2026년 10월 26일

Benzenesulfonyl chloride → 4-Bromo-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/reaction/551037

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물Sodium hydrideHCID 24758—
반응물4-BromoindoleHCID 676494—
용매DimethylformamideHCID 6228—
생성물4-Bromo-1-(phenylsulfonyl)-1H-indoleHCID 22015311—

반응 단계

To a solution of 4-bromoindole (1.00 g, 5.10 mmol) in DMF (50 mL) at ambient temperature was added sodium hydride (220 mg of a 60% dispersion in mineral oil, 5.50 mmol). The reaction mixture was stirred for 5 min, then benzenesulfonyl chloride (901 mg, 5.10 mmol) was added and stirring was continued for 15 min. The reaction was quenched with saturated aqueous NaHCO3 (50 mL) and extracted with CHCl3 (2×75 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 90:10, to give the title compound. MS: m/z=336 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947677B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-c25a0b5ed9ed48e4afd66e9ad4ada2c4
출처 메모uspto-grants-2011_05