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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356975Generated: October 31, 2026

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

https://huagongshe.com/reaction/1356975

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 numberUS06589914B2
Source datasetuspto-grants-2003_07
ORD IDord-46b3fc3081e0436eafad420c6a6c133e
Source noteuspto-grants-2003_07