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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048992Generated: October 26, 2026

Benzoyl Peroxide → Ethyl 2-bromo-2-(3,4-dichlorophenyl)acetate

https://huagongshe.com/reaction/2048992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 3,4-dichlorophenylacetateHCID 2737422—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 2-bromo-2-(3,4-dichlorophenyl)acetateHCID 12717583—

Reaction Steps

In a three-necked flask fitted with a Nichrome stirrer and a reflux condenser is placed 7.0 g of ethyl 3,4-dichlorophenylacetate, 5.9 g of N-bromosuccinimide, 0.1 g of benzoyl peroxide and 150 ml of carbon tetrachloride. The reaction mixture is heated at reflux for 18 hours, cooled and filtered. The carbon tetrachloride filtrate is concentrated under reduced pressure to give a deep orange liquid. Vacuum distillation at 115°-120° C. (0.5 mm) gives ethyl α-bromo-3,4-dichlorophenylacetate as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04196120
Source datasetuspto-grants-1980_04
ORD IDord-5e599ca3fbc74311aedf34fa5f069221
Source noteuspto-grants-1980_04