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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678057Generated: October 25, 2026

4'-Hydroxyacetophenone → 1-[4-(4-Trifluoromethoxybenzyloxy)phenyl]ethanone

https://huagongshe.com/reaction/1678057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-HydroxyacetophenoneHCID 7469—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-4-(trifluoromethoxy)benzeneHCID 142785—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product1-[4-(4-Trifluoromethoxybenzyloxy)phenyl]ethanoneHCID 52561273102.6%

Reaction Steps

A stirred mixture of 4-hydroxyacetophenone (0.9 g, 6.6 mmol), 4-(trifluoromethoxy)benzyl bromide (2.0 g, 7.8 mmol) and potassium carbonate (1.4 g, 10 mmol) in acetone (25 mL) was heated at reflux for 7 hours. The mixture was then cooled, diluted with H2O (50 mL) and extracted with EtOAc (2×100 mL). The organic portions were combined, washed with brine and dried (Na2SO4). Filtration and removal of solvent in vacuo afforded 2.1 g of a crude yellow semi-solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008487B2
Source datasetuspto-grants-2011_08
ORD IDord-261677eb93eb4f75b0e271bf7f802dbc
Source noteuspto-grants-2011_08