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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963477Generated: October 30, 2026

Azobisisobutyronitrile → 2-(Bromomethyl)-1-benzofuran

https://huagongshe.com/reaction/963477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactant2-MethylbenzofuranHCID 20263—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-1-benzofuranHCID 12326316102.6%

Reaction Steps

A suspension of 2-methylbenzofuran (0.708 g) and N-bromosuccinimide (0.963 g) in carbon tetrachloride (10 ml) was heated at reflux temperature for 2.5 hours. To the mixture was added 2,2'-azobis(isobutyronitrile) (0.1 g) and heated at the same temperature for additional 1 hour. The reaction mixture was allowed to cool to room temperature. The resultant precipitates were filtered off by suction. The filtrate was concentrated in vacuo to give 2-bromomethylbenzofuran (1.16 g), which was used in a following reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763437
Source datasetuspto-grants-1998_06
ORD IDord-1c5abc2a5f604653ac7d6f4ed1574675
Source noteuspto-grants-1998_06