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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42446생성일: 2026년 10월 23일

Benzenesulfonyl chloride → 1-Benzenesulfonyl-7-methoxy-1H-indole

https://huagongshe.com/ko/reaction/42446

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물Sodium hydrideHCID 24758—
반응물7-Methoxy-1H-indoleHCID 76660—
용매DimethylformamideHCID 6228—
생성물1-Benzenesulfonyl-7-methoxy-1H-indoleHCID 1177880162.3%

반응 단계

To a cooled (ice water bath) solution of 7-(methyloxy)-1H-indole (3 g, 20.38 mmol) in DMF (100 mL) was added sodium hydride (0.618 g, 24.46 mmol) portionwise. After 15 minutes a solution of benzenesulfonyl chloride (3.94 mL, 30.6 mmol) in 20 ml of DMF was added dropwise. The reaction mixture was stirred at RT for 24 h, at which time it was concentrated. The residue was dissolved in DCM (100 ml) and washed with water and brine, dried over MgSO4, filtered and concentrated. The residue was purified by column chromatography (Biotage; 0% to 100% DCM:Hex; 50 g-HP-silica gel column) to give 3.65 g of the title compound. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 3.65 (s, 3H), 6.60-6.75 (m, 2H), 7.08-7.22 (m, 2H), 7.40-7.62 (m, 3H), 7.77-7.92 (m, 3H). MS (ES) [M+H]+ 288.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536179B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-3330f67c2d1f402b88d3b9a934e454b1
출처 메모uspto-grants-2013_09