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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159763Generated: October 25, 2026

o-Toluenesulfonyl chloride → 4-Bromo-1-(2-methyl-benzenesulfonyl)-1H-indole

https://huagongshe.com/reaction/1159763

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantSodium HydroxideHCID 14798—
Reactant4-BromoindoleHCID 676494—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-Bromo-1-(2-methyl-benzenesulfonyl)-1H-indoleHCID 2201533454%

Reaction Steps

Aq. 2.5 M NaOH (5 mL) was added to a stirring mixture of 4-bromo-1H-indole (1000 mg, 5.3 mmol), 2-methylbenzenesulfonyl chloride (1100 mg, 5.6 mmol) and tetrabutylammonium hydrogen sulfate (173 mg, 0.5 mmol) in DCM (10 mL). The reaction mixture was stirred at ambient temperature overnight. The mixture was diluted with DCM and water and the layers were separated. DCM was washed with water 2 times, dried (MgSO2) and concentrated to give 1.6 g of crude material that was purified using flash chromatography (SiO2, eluent EtOAc:hexane 9:1) giving the title product (1 g, 54%). MS (ESI+) for C15H12BrNO2S m/z 350 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812017B2
Source datasetuspto-grants-2010_10
ORD IDord-3218029980604fa5ab77b0b0aeb011a5
Source noteuspto-grants-2010_10