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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920525Generated: October 31, 2026

Benzyl Alcohol → 1-(4-Benzyloxy-3-trifluoromethyl-phenyl)-ethanone

https://huagongshe.com/reaction/920525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant4'-Fluoro-3'-(trifluoromethyl)acetophenoneHCID 605678—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Benzyloxy-3-trifluoromethyl-phenyl)-ethanoneHCID 6703247972.4%

Reaction Steps

A mixture of benzyl alcohol (10.9 mL; 104.98 mmol) and KOtBu (12.96 g; 115.5 mmol) in THF (500 mL) was heated under reflux for 10 minutes. Subsequently, 4′-fluoro-3′-(trifluoromethyl)acetophenone (21.64 g; 105 mmol) was added and the mixture heated under reflux for another 2 hours. After cooling to RT, the mixture was partitioned between EtOAc and a 5% aqueous NaHCO3 solution. The organic layer was separated, dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by column chromatography (SiO2, Et2O:hexanes 1:2.5) to afford 1-(4-Benzyloxy-3-trifluoromethyl-phenyl)-ethanone (22.37 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273017B2
Source datasetuspto-grants-2016_03
ORD IDord-1d2a2c2718ca41aeaea2d02bd99b3327
Source noteuspto-grants-2016_03