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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692883Generated: October 31, 2026

Bromine → 1-benzenesulfonyl-3-bromo-7-fluoro-1H-indole

https://huagongshe.com/reaction/1692883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Fluoro-1-(phenylsulfonyl)-1H-indoleHCID 11687705—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
Product1-benzenesulfonyl-3-bromo-7-fluoro-1H-indoleHCID 5960352995%

Reaction Steps

To a solution of 1-benzenesulfonyl-7-fluoro-1H-indole (1.00 g, 3.63 mmol) in CCl4 (20 mL) was added a solution of saturated sodium bicarbonate (40 mL) and bromine (0.19 mL, 3.81 mmol) at room temperature. After stirring at room temperature for 16 hours, the reaction was diluted with DCM and water. The organic extract was washed with saturated sodium bicarbonate, 10% aqueous sodium thiosulfate, dried over sodium sulfate, filtered, and concentrated. The product was obtained as an off-white solid (1.22 g, 95%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158625B2
Source datasetuspto-grants-2012_04
ORD IDord-3c5862e76e3f4feb971f97f09d7bf6a5
Source noteuspto-grants-2012_04