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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363104Generated: October 25, 2026

Benzyl Bromide → 4-Bromo-6-chloro-2-methyl-1-benzyloxybenzene

https://huagongshe.com/reaction/363104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-6-chloro-o-cresolHCID 82031—
SolventDimethylformamideHCID 6228—
Product4-Bromo-6-chloro-2-methyl-1-benzyloxybenzeneHCID 1850463090%

Reaction Steps

A solution of 50 g of 4-bromo-6-chloro-2-methylphenol and 42.5 g of benzyl bromide dissolved in 200 ml of N,N-dimethylformamide was stirred at room temperature, to which 37.4 g of potassium carbonate was added, and the mixture was stirred for 12 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure, and the residue was added to 400 ml of diethyl ether, washed with water, dried with anhydrous magnesium sulfate, and concentrated to obtain a crude product. The crude product was subjected to silica gel chromatography, which afforded 63 g of 4-bromo-6-chloro-2-methyl-1-benzyloxybenzene (90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872137
Source datasetuspto-grants-1999_02
ORD IDord-b2c7d625e14b45bf9a8c41ad2155fec3
Source noteuspto-grants-1999_02