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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584771Generated: November 4, 2026

N-bromobutanimide → 5-Bromo-7-bromomethylbenzofuran

https://huagongshe.com/reaction/1584771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Bromo-7-methylbenzofuranHCID 11106653—
CatalystBenzoyl PeroxideHCID 7187—
CatalystTungstenHCID 23964—
SolventCarbon TetrachlorideHCID 5943—
SolventChloroformHCID 6212—
Product5-Bromo-7-bromomethylbenzofuranHCID 19608540113.1%

Reaction Steps

A mixture of 5-bromo-7-methyl-benzofuran (1.01 g), N-bromosuccinimide (1.04 g) and benzoyl peroxide (58 mg) in carbon tetrachloride (10 ml) was heated at reflux for 4 h under a 250 W tungsten lamp. A further portion of benzoyl peroxide (58 mg) was added and heating and irradiation continued for a total of 9 h. The reaction mixture was allowed to cool, diluted with chloroform (30 ml) and washed with 2N sodium hydroxide (40 ml) and then brine (40 ml). The organic phase was dried, filtered and the filtrate evaporated in vacuo to give the title compound as a brown oil (1.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935972
Source datasetuspto-grants-1999_08
ORD IDord-cfb06f118b2846c5987f3d1a1c9fc2da
Source noteuspto-grants-1999_08