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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521489Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 89816088, compound

https://huagongshe.com/reaction/1521489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
Reactant6-(Methylsulfanyl)-1H-indoleHCID 19848917—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
ProductHCID 89816088HCID 8981608859.18%

Reaction Steps

To a solution of 6-(methylthio)-1H-indole (1 g, 6.13 mmol), NaOH (4.90 g, 122.6 mmol) and Bu4NHSO4 (207.8 mg, 0.613 mmol) in dichloromethane (20 mL) was added benzenesulfonyl chloride (1.29 g, 7.36 mmol). The reaction mixture was stirred at rt overnight. The mixture was quenched with water (30 mL) and extracted with dichloromethane (30 mL×3). The combined organic layers were dried over anhydrous sodium sulfate, filtered, concentrated and purified by column chromatography on silica gel eluted with PE/EtOAc 10:1 to afford 6-(methylthio)-1-(phenylsulfonyl)-1H-indole (1.1 g, 59.18% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073931B2
Source datasetuspto-grants-2015_07
ORD IDord-c92825280dde43a2b8bc5e32b60e0955
Source noteuspto-grants-2015_07