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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478197Generated: October 30, 2026

Water → 3-Bromo-1-(P-toluenesulfonyl)indole

https://huagongshe.com/reaction/478197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
Reactant3-Bromo-1h-indoleHCID 2763277—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventBenzeneHCID 241—
Product3-Bromo-1-(P-toluenesulfonyl)indoleHCID 1121027496%

Reaction Steps

To a solution of 3-bromoindole (prepared according to the method described in Synthesis, 1096(1982)) (196 mg, 1.0 mmol) and tosyl chloride (286 mg, 1.5 mmol) in benzene (4.5 mL) was added tetra-n-butylammonium hydrogensulfate (34 mg, 0.1 mmol) and a 5.0% aqueous sodium hydroxide (1.0 mL), and the resulting mixture was refluxed for 1 hour. After the reaction solution was cooled to room temperature, water was added to the reaction solution, and the resulting mixture was extracted with chloroform. After drying over anhydrous sodium sulfate, the chloroform layer was concentrated, and the resulting crude product was purified by column chromatography on a silica gel (eluent; hexane:ethyl acetate=6:1) to afford the title compound (335 mg, yield: 96%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642228B1
Source datasetuspto-grants-2003_11
ORD IDord-d4eccb9a4fc145d0b357794e9d169fb4
Source noteuspto-grants-2003_11