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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643118Generated: October 29, 2026

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

https://huagongshe.com/reaction/643118

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) benzylbromide in 450 mL acetonitrile was refluxed for 3 h, cooled to RT and evaporated down i.vac. The residue was combined with EtOAc, the organic phase was washed with water and saturated NaCl solution, dried over Na2SO4 and evaporated down i.vac.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696209B2
Source datasetuspto-grants-2010_04
ORD IDord-7ed29cdc0eda4984ad8d2aeb9fbd574b
Source noteuspto-grants-2010_04