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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159785Generated: November 4, 2026

Benzenesulfonyl chloride → 1-(benzenesulfonyl)-4-bromo-6-fluoro-1H-indole

https://huagongshe.com/reaction/1159785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromo-6-fluoro-1H-indoleHCID 24728173—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
Product1-(benzenesulfonyl)-4-bromo-6-fluoro-1H-indoleHCID 68716114130.3%

Reaction Steps

Aq. 4 M NaOH (5 mL) was added to a stirring mixture of 4-bromo-6-fluoro-1H-indole (500 mg, 2.34 mmol; Intermediate 35), benzenesulfonyl chloride (329 μL g, 2.57 mmol) and tetrabutylammonium hydrogen sulfate (78 mg, 0.23 mmol) in DCM (30 mL). The reaction mixture was stirred 1 h, combined with an earlier batch of this intermediate (followed this experimental and starting with 4-bromo-6-fluoro-1H-indole, 152 mg, 0.71 mmol; Intermediate 35), washed twice with water, dried and concentrated. The product (1.08 g, 100%) was obtained as a beige solid. MS (ESI+) for C14H9BrFNO2S m/z 354 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812017B2
Source datasetuspto-grants-2010_10
ORD IDord-bf922ae7970c4c25b4f5ca2f6ecdba4e
Source noteuspto-grants-2010_10