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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167098Generated: October 26, 2026

Triethylamine → 1-Benzyl-4-(4'-trifluoromethylbiphenyl-2-carbonylamino)piperidine

https://huagongshe.com/reaction/1167098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
Reactant4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chlorideHCID 11066000—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-4-(4'-trifluoromethylbiphenyl-2-carbonylamino)piperidineHCID 22995692—

Reaction Steps

34.1 g (0.12 mol) of 4′-trifluoromethyl-biphenyl-2-carboxylic acid chloride, dissolved in 300 ml of dichloromethane, are added dropwise at 15 to 20° C. to a solution of 22.43 ml (0.11 mol) of 4-amino-1-benzyl-piperidine and 42.97 ml (0.31 mol) of triethylamine in 600 ml of dichloromethane. The mixture is stirred for 14 hours at ambient temperature. The reaction solution is diluted with 300 ml of dichloromethane and extracted with a mixture of 1N sodium hydrogen carbonate solution and 1N sodium hydroxide solution. The organic phase is dried over sodium sulphate and the solvent is eliminated. The residue is recrystallised from 650 ml ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617325B1
Source datasetuspto-grants-2003_09
ORD IDord-202a530e186a44ae9223cb8241a87ba6
Source noteuspto-grants-2003_09