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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988185Generated: November 4, 2026

Benzoyl Peroxide → 7-(bromomethyl)-4-(4-fluorophenyl)-2H-chromen-2-one

https://huagongshe.com/reaction/1988185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant4-(4-fluorophenyl)-7-methyl-2H-chromen-2-oneHCID 57729246—
SolventCarbon TetrachlorideHCID 5943—
Product7-(bromomethyl)-4-(4-fluorophenyl)-2H-chromen-2-oneHCID 19426963—

Reaction Steps

A mixture of 4-(4-fluorophenyl)-7-methyl-2H-chromen-2-one (24.0, 94.3 mmol), NBS (18.5 g, 103.8 mmol) and benzoyl peroxide (1.14 g, 4.72 mmol) in 470 mL of CCl4 was brought to reflux. The solution was left overnight at reflux and then filtered hot. Once cooled to rt the solvent was removed, the compound was dissolved in CH2Cl2 and a purification was done with a small pad of silica gel using hexane-EtOAc (8/2) to (1/1). The solvent was removed and the solid triturated with hexane-EtOAc and filtered to give the title compound. The remaining solvent was removed to give additional compound contaminated with some starting material and dibromo compound. 1H NMR (400 MHz, acetone-d6): δ 7.67 (2H, m), 7.55 (1H, s), 7.50 (1H, d), 7.40 (3H, m), 6.40 (1H, s) and 4.75 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553973B2
Source datasetuspto-grants-2009_06
ORD IDord-286febfb7e924532958035e060139d3c
Source noteuspto-grants-2009_06