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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377728Generated: October 30, 2026

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

https://huagongshe.com/reaction/377728

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 numberUS06028100
Source datasetuspto-grants-2000_02
ORD IDord-751427f97a8c4b999634f05fad2a5e11
Source noteuspto-grants-2000_02