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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441685Generated: October 30, 2026

Azobisisobutyronitrile → 4-Bromomethyl-2-trifluoromethylbenzonitrile

https://huagongshe.com/reaction/1441685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Methyl-2-(trifluoromethyl)benzonitrileHCID 2775597—
SolventCarbon TetrachlorideHCID 5943—
Product4-Bromomethyl-2-trifluoromethylbenzonitrileHCID 59164585157.1%

Reaction Steps

To a refluxing mixture of 5.0 g 4-Methyl-2-(trifluoromethyl)benzonitrile in 50 ml tetrachloromethane were added a mixture of 5.77 g N-bromosuccinimide and 1.77 g 2,2′-azobis(2-methylpropionitrile). The reaction mixture was heated under reflux for three hours. The reaction mixture was filtered through a pad of celite and the solvent was removed in vacuo to obtain 11.2 g crude 4-Bromomethyl-2-trifluoromethyl-benzonitrile (impurified with the dibromo product) as a white solid. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655679B2
Source datasetuspto-grants-2010_02
ORD IDord-f1dbe9fd966e46c483507ca4ba370b6e
Source noteuspto-grants-2010_02