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HRID 551037作成日:2026年10月26日

Benzenesulfonyl chloride → 4-Bromo-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/reaction/551037

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4-BromoindoleHCID 676494—
溶媒DimethylformamideHCID 6228—
生成物4-Bromo-1-(phenylsulfonyl)-1H-indoleHCID 22015311—

反応手順

To a solution of 4-bromoindole (1.00 g, 5.10 mmol) in DMF (50 mL) at ambient temperature was added sodium hydride (220 mg of a 60% dispersion in mineral oil, 5.50 mmol). The reaction mixture was stirred for 5 min, then benzenesulfonyl chloride (901 mg, 5.10 mmol) was added and stirring was continued for 15 min. The reaction was quenched with saturated aqueous NaHCO3 (50 mL) and extracted with CHCl3 (2×75 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 90:10, to give the title compound. MS: m/z=336 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947677B2
出典データセットuspto-grants-2011_05
ORD IDord-c25a0b5ed9ed48e4afd66e9ad4ada2c4
出典メモuspto-grants-2011_05