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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281642Generated: November 2, 2026

Benzoyl Peroxide → HCID 18421399, compound

https://huagongshe.com/reaction/1281642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant225379-14-6HCID 854734—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 18421399HCID 18421399—

Reaction Steps

A mixture of 7-acetoxy-3,4,8-trimethylcoumarin (6.22 g, 25.3 mmol), N-bromosuccinimide (4.61 g, 25.9 mmol) and benzoyl peroxide (390 mg) were refluxed in carbon tetrachloride for 3.5 hours. The mixture was cooled to room temperature and partitioned between CH2Cl2 and water. The organic layer was separated and washed with water several times, then washed with brine. The organic layer was then dried with anhydrous sodium sulfate and evaporated to give crude product (11.8 g) which was recrystallized twice in toluene to give 7-acetoxy-3-bromomethyl-4,8-dimethylcoumarin, a white crystalline solid (4.86 g, 59%). 1H NMR (CDCl3): δ7.54 (d; J=8.8 Hz, 1H), 7.05 (d, J=8.8 Hz, 1H), 4.57 (s, 2H), 2.50 (s, 3H), 2.37 (s, 3H), 2.28 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455286B1
Source datasetuspto-grants-2002_09
ORD IDord-04952936b8da48c48025c43cd2dc3d17
Source noteuspto-grants-2002_09