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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129089Generated: October 29, 2026

Triethylamine → 4-[4-(2-Oxazolin-2-yl)benzylidene]-1-(4-trifluoromethylbenzoyl)piperidine

https://huagongshe.com/reaction/129089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
Reactant4-[4-(2-Oxazolin-2-yl)benzylidene]piperidineHCID 15231403—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-[4-(2-Oxazolin-2-yl)benzylidene]-1-(4-trifluoromethylbenzoyl)piperidineHCID 15231386—

Reaction Steps

120 mg (0.5 mmol) of 4-[4-(2-oxazolin-2-yl)benzylidene]piperidine and 75 mg (0.75 mmol) of triethylamine in 3 ml of ethyl acetate and 2 ml of methylene chloride are cooled to -5° to -10° C. and 104.3 mg (0.5 mmol) of 4-trifluoromethylbenzoyl chloride are added. The mixture is stirred at ambient temperature for 1.5 hours, diluted with ethyl acetate, washed successively with water, 2N sodium hydroxide solution and saturated saline solution, dried and evaporated down. 115 mg (56% of theory) of the title compound of melting point 142° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466687
Source datasetuspto-grants-1995_11
ORD IDord-3895126c1b6c4938850e9278ca15b188
Source noteuspto-grants-1995_11