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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378883Generated: November 1, 2026

Ethanol → HCID 22908542, compound

https://huagongshe.com/reaction/1378883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 22908554HCID 22908554—
SolventHCID 178418361HCID 178418361—
ProductHCID 22908542HCID 2290854299.9%

Reaction Steps

A mixture of (4-trifluoromethoxyphenyl)cyclohexen-4-one ethyleneketal (43.3 g, 0.144 mol), ethanol (200 ml), ethyl acetate (50 ml) and Pa-C (2 g) was stirred at room temperature for 10 hours in hydrogen atmosphere (at that time, hydrogen (3.59 l) was consumed), filtering off the catalyst from the reaction solution, distilling off the solvent under reduced pressure, to obtain 4-(4-trifluoromethoxyphenyl)cyclohexanone ethyleneketal (43.5 g) (m.p. 41.2° C.), adding thereto formic acid (250 ml), heating the mixture under reflux for 2.5 hours, feeding the reaction substance into water, extracting with a mixed solvent of toluene (400 ml) with ethyl acetate (100 ml), twice washing the resulting orgnaic layer with water, drying over anhydrous MgSO4, filtering off anhydrous MgSO4, distilling off the solvent under reduced pressure and subjecting the resulting residue to column chromatography (silica gel, eluent: toluene), to obtain 4-(4-trifluoromethoxyphenyl)cyclohexanone (20.7 g). Yield: 47%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670085
Source datasetuspto-grants-1997_09
ORD IDord-fe1c7ed70f804864b1846505aa37b2a4
Source noteuspto-grants-1997_09