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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440538Generated: October 25, 2026

4-Chloro-3-methylphenol → 2-(Bromomethyl)-1-chloro-4-methoxybenzene

https://huagongshe.com/reaction/440538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-3-methylphenolHCID 1732—
ReactantMethyl iodideHCID 6328—
ReactantBenzoyl PeroxideHCID 7187—
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
SolventAcetoneHCID 180—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-1-chloro-4-methoxybenzeneHCID 12484533—

Reaction Steps

Methyl iodide (110 g was added dropwise to a stirred solution of 4-chloro-3-methylphenol (100 g) and potassium carbonate (194 g) in acetone (500 ml). The mixture was stirred for 1.5 hours. Methyl iodide (142 g) was added and the mixture stirred for a further hour. Solvent was removed by evaporation and the residue partitioned between water and ethyl acetate. The organic layer yielded an oil which was heated under reflux for 2 hours with N-bromosuccinimide (119 g) and benzoyl peroxide (1 g) in carbon tetrachloride (250 ml). The mixture was cooled, filtered and the filtrate concentrated to give a residue which was distilled under high vacuum. The fractions collected between 88° and 94° C./0.4 mbar were recrystallised from petroleum ether (b.p. 60°-80° C.) to give 2-chloro-5-methoxy benzyl bromide, m.p. 51°-52° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519034
Source datasetuspto-grants-1996_05
ORD IDord-1d535b203d78433f9de20e65f2021495
Source noteuspto-grants-1996_05