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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345032Generated: October 30, 2026

N-bromobutanimide → 2-(Bromomethyl)-5-nitro-1-benzofuran

https://huagongshe.com/reaction/345032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methyl-5-nitrobenzofuranHCID 4487453—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-5-nitro-1-benzofuranHCID 1141417952.3%

Reaction Steps

N-Bromosuccinimide (1.1 g. 6.2 mmole) was added portionwise to a solution of 2-methyl-5-nitrobenzofuran (1.0 g, 5.6 mmole) and benzoyl peroxide (50 mg) in carbon tetrachloride (50 ml) and the reaction mixture was heated at reflux temperature for 6 hours in the presence of bright light. The reaction mixture was then cooled, filtered and the filtrate evaporated to dryness. The residue was recrystallised from petroleum ether to give the title compound yield 0.75 g, m.p. 96°-98°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055473
Source datasetuspto-grants-1991_10
ORD IDord-ca4cca6f499844f78260077a2583c2bf
Source noteuspto-grants-1991_10