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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159781Generated: November 2, 2026

Benzenesulfonyl chloride → 4-Bromo-6-methoxy-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/reaction/1159781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
Reactant4-bromo-6-methoxy-1H-indoleHCID 24728026—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
Product4-Bromo-6-methoxy-1-(phenylsulfonyl)-1H-indoleHCID 68718624—

Reaction Steps

4-Bromo-6-methoxy indole (0.07 g, 0.3 mmol) was dissolved in dry dichloromethane (4 mL) and benzenesulphonyl chloride (0.06 g, 0.3 mmol), tetrabutylammonium hydrogen sulphate (0.01 g, 0.01 mmol) and 4N NaOH (0.5 mL) were added and the mixture was stirred at rt for 50 min. The mixture was extracted with water (2×4 mL), dried (Na2SO4) and evaporated. The crude product was combined with an earlier batch of this intermediate (followed this experimental and starting with 4-bromo-6-methoxy indole (0.35 g, 1.5 mmol). MS (ESI+) for C15H12BrNO3S m/z 366 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812017B2
Source datasetuspto-grants-2010_10
ORD IDord-e6b77c22118a43229d702192b50cc658
Source noteuspto-grants-2010_10