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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226008Generated: October 27, 2026

N-bromobutanimide → 2-Bromo-5-fluoro-3-methylbenzo[b]thiophene

https://huagongshe.com/reaction/226008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Fluoro-3-methyl-benzo[b]thiopheneHCID 596828—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-Bromo-5-fluoro-3-methylbenzo[b]thiopheneHCID 66721202—

Reaction Conditions

Temperature40 °C

Reaction Steps

A mechanically-stirred solution of 5-fluoro-3-methylbenzo[b]thiophene (50.32 g, 0.303 mol, 1.0 equiv) in acetonitrile (350 mL) is treated with NBS (56.32 g, 0.318 mol, 1.05 equiv). An initial endotherm reduces the reaction temperature to 17° C. A subsequent exotherm then increases the reaction temperature to 40° C. over a 10 min. period, at which time the reaction is cooled to 18-20° C. by application of an ice water bath. The reaction is stirred at RT for an additional 35 min. and the resultant slurry is slowly diluted with water (350 mL). The slurry is stirred for 10 min and the product is filtered, washed with 50:50 acetonitrile:water (100 mL) and dried to a colorless crystalline solid (65.56 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557103B2
Source datasetuspto-grants-2009_07
ORD IDord-d7980c324e7e437d8e60bd8c7dc6666b
Source noteuspto-grants-2009_07