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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323685Generated: October 26, 2026

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

https://huagongshe.com/reaction/323685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-ethyl-6-methylphenolHCID 22006838—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2-ethyl-6-methyl-1-benzyloxybenzeneHCID 2200681397%

Reaction Steps

To a mixture of 26 g of 4-bromo-2-ethyl-6-methylphenol, 24.8 g of benzyl bromide and 200 ml of N,N-dimethylformamide was added 21.7 g of potassium carbonate, while stirring at room temperature. After stirring at room temperature for 24 hours, the reaction mixture was poured into ice water, and extracted twice with 500 ml of diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 35.6 g of 4-bromo-2-ethyl-6-methyl-1-benzyloxybenzene (97% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214835B1
Source datasetuspto-grants-2001_04
ORD IDord-37dbb46dddc04e7aa80bf91a2014ba12
Source noteuspto-grants-2001_04