Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828703Generated: October 26, 2026

1-Cyclohexyl-4-(4-methoxy-benzyloxymethyl)-2-trifluoromethyl-benzene → [4-Cyclohexyl-3-(trifluoromethyl)phenyl]methanol

https://huagongshe.com/reaction/1828703

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Cyclohexyl-4-(4-methoxy-benzyloxymethyl)-2-trifluoromethyl-benzeneHCID 22057736—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
SolventEthyl AcetateHCID 8857—
Product[4-Cyclohexyl-3-(trifluoromethyl)phenyl]methanolHCID 22057748—

Reaction Steps

The obtained 1-cyclohexyl-4-(4-methoxy-benzyloxymethyl)-2-trifluoromethyl-benzene is dissolved in a mixture of TFA and DCM (8 mL, 1:1 v/v). After stirring at room temperature for 2 h, all volatile materials are evaporated and the residue obtained is dissolved in EtOAc and washed with saturated aqueous NaHCO3. The organic layer is separated, washed with saturated aqueous NaCl and dried over Na2SO4. After concentration, the residue is purified by silica gel chromatography (20% ethyl acetate in hexanes) to give (4-cyclohexyl-3-trifluoromethyl-phenyl)-methanol as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060697B2
Source datasetuspto-grants-2006_06
ORD IDord-0a86972aced5457e8484d1df143603d7
Source noteuspto-grants-2006_06