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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681941Generated: October 25, 2026

Azobisisobutyronitrile → 2-(Bromomethyl)-3-chlorobenzonitrile

https://huagongshe.com/reaction/1681941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Chloro-2-methylbenzonitrileHCID 521508—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
Product2-(Bromomethyl)-3-chlorobenzonitrileHCID 1498051046%

Reaction Steps

To a refluxing solution of 3-chloro-2-methylbenzonitrile (2.0 g,13.2 mmol) in 20 mL of CCl4 was added 2.6 g (14.4 mmol, 1.1 eq) of N-bromosuccinimide and 0.2 g of AIBN. The solution was refluxed for 3 hours and then cooled, diluted with 500 mL of CH2Cl2 and washed with 200 mL of H2O and 200 mL of brine. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. The resultant oil was flash chromatographed with 5:1 hexane/ethyl acetate to yield the titled compound (1.4 g, 46%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175164
Source datasetuspto-grants-1992_12
ORD IDord-3b546b47d34b473092825a58018d0021
Source noteuspto-grants-1992_12