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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577498Generated: October 28, 2026

Azobisisobutyronitrile → Ethyl 2-(bromomethyl)-3,6-dichlorobenzoate

https://huagongshe.com/reaction/577498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 3,6-dichloro-2-methylbenzoateHCID 86723723—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(bromomethyl)-3,6-dichlorobenzoateHCID 86723724100%

Reaction Steps

A solution of 3,6-dichloro-2-methylbenzoate (253b, 120 g, 0.52 mol) and N-bromosuccinimide (147 g, 0.82 mol) in chloroform (1 L) was treated with azobisisobutyronitrile (25.3 g, 0.15 mol) and the mixture refluxed overnight. After cooling to room temperature, the mixture was diluted with dichloromethane (800 mL) and washed with water (1.2 L). The aqueous layer was extracted with dichloromethane (800 mL). The combined organic extracts were washed with saturated aqueous sodium chloride solution (1.5 L), dried over sodium sulfate, and concentrated in vacuo to give ethyl 2-(bromomethyl)-3,6-dichlorobenzoate (253c, 160 g, 100% yield) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040515B2
Source datasetuspto-grants-2015_05
ORD IDord-3d86e46f619942e29e00f8256a694502
Source noteuspto-grants-2015_05