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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666735Generated: October 31, 2026

Water → 2-bromo-1H-indole

https://huagongshe.com/reaction/1666735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromineHCID 24408—
ReactantEthyl 1-(benzenesulfonyl)indole-2-carboxylateHCID 506886—
SolventDimethylformamideHCID 6228—
Product2-bromo-1H-indoleHCID 11805631—

Reaction Steps

To a stirred solution of ethyl 1-phenylsulfonylindole-2-carboxylate (1 eq.) in DMF (2.5 ml/mmol) under N2, was added a solution of bromine (4 eq.) in DMF (0.5 ml/mmol). This reaction mixture was stirred at room temperature for about 4 hours, following which water was added and the mixture was extracted with dichloromethane (×3). The organic layer was washed with a saturated solution of Na2SO5, dried and evaporated to give a crude yellow oil. Purification by chromatography on silica gel (eluent:C6H12/EtOAc 9/1) afforded 3-brominated indole 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044091B2
Source datasetuspto-grants-2011_10
ORD IDord-807d5efe116d4f3eb19b6d54a004332d
Source noteuspto-grants-2011_10