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HRID 2165643作成日:2026年10月26日

Benzenesulfonyl chloride → 1H-Indole, 3-acetyl-1-(phenylsulfonyl)-

https://huagongshe.com/reaction/2165643

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3-AcetylindoleHCID 12802—
反応物Potassium HydroxideHCID 14797—
反応物Ammonium ChlorideHCID 25517—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物1H-Indole, 3-acetyl-1-(phenylsulfonyl)-HCID 848535—

反応条件

温度0 °C

反応手順

To a solution of 41.39 g of 3-acetyl indole in 300 ml of dimethyl sulfoxide at 0° C. was added a solution of 18.6 g of potassium hydroxide in 20 ml of water. This mixture was stirred at 0° C. for 2 hours, then 47.6 ml of benzenesulfonyl chloride was added dropwise over 40 minutes. The mixture was stirred for an additional 30 minutes, then poured into aqueous ammonium chloride and extracted several times with ether. The ether extracts were combined, washed with water, dried and evaporated, giving 59.8 g of 3-acetyl-N-phenylsulfonyl indole.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04940710
出典データセットuspto-grants-1990_07
ORD IDord-2b93cceae6c045508a234743f73a4884
出典メモuspto-grants-1990_07