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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886463Generated: October 25, 2026

Azobisisobutyronitrile → 2-(Bromomethyl)-3-chlorobenzonitrile

https://huagongshe.com/reaction/1886463

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 numberUS05151435
Source datasetuspto-grants-1992_09
ORD IDord-4280b87baf5245388b53ad9905af87bd
Source noteuspto-grants-1992_09