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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204675Generated: November 1, 2026

Benzoyl Peroxide → Methyl 2-(acetyloxy)-5-bromo-4-(bromomethyl)benzoate

https://huagongshe.com/reaction/2204675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-(acetyloxy)-5-bromo-4-methylbenzoateHCID 66611776—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 2-(acetyloxy)-5-bromo-4-(bromomethyl)benzoateHCID 66611269—

Reaction Steps

NBS (0.71 g, 4.01 mmol) and benzoyl peroxide (0.07 g, 0.20 mmol) were added to a solution of methyl 2-(acetyloxy)-5-bromo-4-methylbenzoate (may be prepared as described in Description 3; 1.15 g, 4.01 mmol) in carbon tetrachloride (20 ml). The mixture was heated at reflux for 18 hours, cooled and the solvent removed in vacuo. Purification by SP4 (10-20% ethyl acetate/hexane) yielded the title compound as a pale yellow oil. 1.38 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365551B2
Source datasetuspto-grants-2016_06
ORD IDord-9ebb55aa8dd94dec93ecde9ca6d82ae5
Source noteuspto-grants-2016_06