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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129092Generated: October 28, 2026

Ethyl Acetate → 4-[4-(2-Oxazolin-2-yl)benzyl]-1-(4-trifluoromethylbenzoyl)piperidine

https://huagongshe.com/reaction/129092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-[4-(2-Oxazolin-2-yl)benzylidene]-1-(4-trifluoromethylbenzoyl)piperidineHCID 15231386—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product4-[4-(2-Oxazolin-2-yl)benzyl]-1-(4-trifluoromethylbenzoyl)piperidineHCID 15231394—

Reaction Steps

441 mg (1 mmol) of 4-[4-(2-oxazolin-2-yl)benzylidene]-1-(4-trifluoromethylbenzoyl)piperidine are hydrogenated (ambient temperature, 30 minutes, hydrogen pressure 50 psi) in 10 ml of anhydrous ethanol and 2.5 ml of ethyl acetate in the presence of 0.5 g of palladium-carbon (10%). The catalyst is then suction-filtered, the filtrate is evaporated under reduced pressure at a bath temperature of 50° C. and the residue is purified by column chromatography (Silica gel; ethyl acetate). 200 mg (48% of theory) of the title compound of melting point 115° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466687
Source datasetuspto-grants-1995_11
ORD IDord-86e54884df594b6f9f2f01f4ed97cdcc
Source noteuspto-grants-1995_11