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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197365Generated: October 30, 2026

Benzoyl Peroxide → Benzoic acid, 4-bromo-3-(bromomethyl)-, ethyl ester

https://huagongshe.com/reaction/2197365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 4-bromo-3-methylbenzoateHCID 21729626—
SolventCarbon TetrachlorideHCID 5943—
ProductBenzoic acid, 4-bromo-3-(bromomethyl)-, ethyl esterHCID 22574851—

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Bromo-3-methyl-benzoic acid ethyl ester (18.24 g, 75.4 mmol), N-bromosuccinimide (14.1 g, 79.2 mmol), and benzoyl peroxide (0.9 g, 3.77 mmol) were combined in CCl4, and the reaction was heated to 80° C. and stirred with a halogen desk lamp shining on it for 6 hours. The mixture was concentrated and partitioned between CH2Cl2 and H2O. The organic layer was separated and washed with H2O and brine, and then dried and concentrated. The residue was triturated with hexane (3×50 mL) and dried to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338484B2
Source datasetuspto-grants-2012_12
ORD IDord-716171413c9e43b4a67ceb234f7b27f7
Source noteuspto-grants-2012_12