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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2086937생성일: 2026년 10월 26일

Benzenesulfonyl chloride → 1-(Phenylsulfonyl)-1,5,6,7-tetrahydro-4H-indol-4-one

https://huagongshe.com/reaction/2086937

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물Sodium hydrideHCID 24758—
반응물1,5,6,7-Tetrahydro-4H-indol-4-oneHCID 280229—
용매TetrahydrofuranHCID 8028—
생성물1-(Phenylsulfonyl)-1,5,6,7-tetrahydro-4H-indol-4-oneHCID 1343770985%

반응 단계

A stirred solution of 1,5,6,7-tetrahydro-4H-indol-4-one (5.0 g, 37.0 mmol) in THF is treated portionwise with NaH (60% dispersion in mineral oil, 1.5 g, 37.0 mmol) under N2 at room temperature, stirred for 0.5 hr, treated with benzene sulfonyl chloride (4.7 ml, 37.0 mmol), stirred for 24 hr, quenched with water and diluted with EtOAc. The phases are separated. The organic phase is washed sequentially with water and brine, dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by flash chromatography (silica gel, EtOAc/hexanes, 1/1 as eluent) to afford the title product as an off-white solid, 8.72 g (85% yield), mp 108-110° C., identified by NMR and mass spectral analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06727270B2
출처 데이터셋uspto-grants-2004_04
ORD IDord-8094538fe8ee497da0857f8a1ee97d97
출처 메모uspto-grants-2004_04