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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563673Generated: October 30, 2026

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

https://huagongshe.com/reaction/563673

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 numberUS08067445B2
Source datasetuspto-grants-2011_11
ORD IDord-2040aa659f424cf8861a17f9d877d5dc
Source noteuspto-grants-2011_11