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HRID 2086937作成日:2026年10月26日

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

https://huagongshe.com/reaction/2086937

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chlorideHCID 7369—
反応物Sodium hydrideHCID 24758—
反応物1,5,6,7-Tetrahydro-4H-indol-4-oneHCID 280229—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Phenylsulfonyl)-1,5,6,7-tetrahydro-4H-indol-4-oneHCID 1343770985%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06727270B2
出典データセットuspto-grants-2004_04
ORD IDord-8094538fe8ee497da0857f8a1ee97d97
出典メモuspto-grants-2004_04