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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444539Generated: October 29, 2026

Benzoyl Peroxide → 4-Fluoro-3-methoxybenzyl bromide

https://huagongshe.com/reaction/1444539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-5-methylanisoleHCID 2737372—
SolventCarbon TetrachlorideHCID 5943—
Product4-Fluoro-3-methoxybenzyl bromideHCID 17989267—

Reaction Steps

41.7 g (297.54 mmol) of 2-fluoro-5-methylanisole is refluxed overnight with 59.9 g (327.48 mmol) of N-bromosuccinimide and 145 mg of benzoyl peroxide in 945 ml of carbon tetrachloride. The reaction mixture is filtered through a glass-fiber filter, and after the solvent is spun off, the residue (72.85 g>100%) is incorporated in crude form into the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662821B2
Source datasetuspto-grants-2010_02
ORD IDord-22e35015fa83478ca344aa87150ef1a0
Source noteuspto-grants-2010_02