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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481976Generated: October 31, 2026

N-bromobutanimide → 5-Bromo-3-(bromomethyl)-1-benzothiophene

https://huagongshe.com/reaction/481976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Bromo-3-methyl-1-benzothiopheneHCID 14175764—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product5-Bromo-3-(bromomethyl)-1-benzothiopheneHCID 2179041174%

Reaction Steps

A solution of 4.30 gm (18.9 mMol) 5-bromo-3-methylbenzothiophene, 0.25 gm (1.03 mMol) benzoylperoxide, and 3.37 gm (18.9 mMol) N-bromosuccinimide in 50 mL carbon tetrachloride was heated at reflux for 3 hours. The reaction mixture was cooled to room temperature, filtered and the filtrate concentrated under reduced pressure. The residue was subjected to flash silica gel chromatography, eluting with hexane. Fractions containing the desired compound were combined and concentrated under reduced pressure to provide 4.28 gm (74%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792763
Source datasetuspto-grants-1998_08
ORD IDord-776cab91e17c4389b641455b46db93a8
Source noteuspto-grants-1998_08