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HRID 736980생성일: 2026년 10월 25일

o-Toluenesulfonyl chloride → 1-{1-[(4-Methylphenyl)sulfonyl]-1H-indol-3-yl}ethanone

https://huagongshe.com/reaction/736980

반응식

참여 물질

역할이름HCID투입량
반응물o-Toluenesulfonyl chlorideHCID 8623—
반응물3-AcetylindoleHCID 12802—
반응물Water ethylacetateHCID 22728543—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
생성물1-{1-[(4-Methylphenyl)sulfonyl]-1H-indol-3-yl}ethanoneHCID 35779478%

반응 단계

Add 1.0 M t-BuOK (3.0 mL, 0.003 mol) to a stirring solution of 3-acetyl indole (0.478 g, 0.0030 mol) in dry DMF (20 mL) under N2 at ambient temperature and stir for 30 min. Add toluenesulfonyl chloride to this solution and stir the resulting mixture overnight. Pour the reaction into EtOAc—H2O, separate the organic layer and extract several times with H2O wash with brine, dry (MgSO4), filter, and evaporate on the rotary evaporator. Chromatograph on the ISCO eluting with a gradient hexane-EtOAc (0-100%) over 30 minutes to give 0.73 g (78%) of the title compound as a solid: 1H (CDCl3). δ 7.8 (d, 1H), 8.2 (s, 1H), 7.9 (d, 1H), 7.7 (d, 2H), 7.4 (m, 2H), 7.3 (d, 2H), 2.6 (s, 3H), 2.4 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07595339B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-0dea3151871241489e90aa87c1b82c56
출처 메모uspto-grants-2009_09