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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187637Generated: October 26, 2026

Benzoyl Peroxide → 2-(Bromomethyl)-5-chloro-1-benzothiophene

https://huagongshe.com/reaction/2187637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 2747689HCID 2747689—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-5-chloro-1-benzothiopheneHCID 1364260697.2%

Reaction Steps

A solution of 2.73 g (14.95 mmol) 5-chloro-2-methylbenzothiophene and 2.67 g (15.0 mmol) NBS in 100 ml carbon tetrachloride was heated to 70° C. and a catalytic amount of dibenzoyl peroxide was added. After 30 min reflux solids were removed by filtration. The solvent was removed in vacuo and the residue was suspended in 100 ml hot hexane and filtered. The filtrate was evaporated to dryness to give 3.8 g (97%) of the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410562B1
Source datasetuspto-grants-2002_06
ORD IDord-ad5f07453d094c149062c1a63b92adea
Source noteuspto-grants-2002_06