Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730694Generated: October 29, 2026

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

https://huagongshe.com/reaction/730694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-ethyl-6-methylphenolHCID 22006838—
SolventAcetonitrileHCID 6342—
Product4-Bromo-2-ethyl-6-methyl-1-benzyloxybenzeneHCID 22006813—

Reaction Steps

A suspension of 39.8 g (185 mmol) 4-bromo-2-ethyl-6-methyl-phenol, 63.9 g (0.46 mmol) K2CO3 and 22.0 mL (185 mmol) benzyl bromide in 450 mL acetonitrile was refluxed for 3 h, cooled to RT and concentrated by evaporation i. vac. The residue was combined with EtOAc, the organic phase was washed with water and saturated NaCl solution, dried on Na2SO4 and concentrated by evaporation i. vac.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582625B2
Source datasetuspto-grants-2009_09
ORD IDord-760f3dae8aef4473948faaf95e702195
Source noteuspto-grants-2009_09