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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422483Generated: November 1, 2026

Benzoyl Peroxide → 7-(bromomethyl)-4-(3-fluorophenyl)-2H-chromen-2-one

https://huagongshe.com/reaction/2422483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant4-(3-fluorophenyl)-7-methyl-2H-chromen-2-oneHCID 56971674—
SolventCarbon TetrachlorideHCID 5943—
Product7-(bromomethyl)-4-(3-fluorophenyl)-2H-chromen-2-oneHCID 59774861—

Reaction Steps

To a solution of 4-(3-fluorophenyl)-7-methyl-2H-chromen-2-one (1.25 g, 4.9 mmol) in carbontetrachloride (30 mL), N-bromosuccinimide (963 mg, 5.41 mmol) and benzoylperoxide (60 mg, 0.25 mmol) were added. The reaction was then stirred overnight at reflux. After cooling, the reaction mixture was concentrated under reduced pressure. The crude residue obtained was purified on a short column of silica gel (eluting with CH2Cl2). The filtrate was concentrated and the solid obtained was swished in a mixture of CH2Cl2/hexanes. The title product was collected by filtration. 1H NMR (400 MHz, acetone-d6): 7.72-7.6 (m, 1H), 7.55 (s, 1H), 7.47 (s, 1H), 7.45-7.3 (m, 4H), 6.4 (s, 1H), 4.78 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960409B2
Source datasetuspto-grants-2011_06
ORD IDord-4ec1fc7ea3c547509c877eda9fe6c16d
Source noteuspto-grants-2011_06