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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189970Generated: October 30, 2026

Trifluoroacetic acid → 4-(4-fluorophenyl)-N-[(1S)-1-(4-fluorophenyl)ethyl]piperidine-4-carboxamide;2,2,2-trifluoroacetic acid

https://huagongshe.com/reaction/2189970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(4-fluoro-phenyl)-4-[(S)-1-(4-fluoro-phenyl)-ethylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 66671195—
SolventDichloromethaneHCID 6344—
Product4-(4-fluorophenyl)-N-[(1S)-1-(4-fluorophenyl)ethyl]piperidine-4-carboxamide;2,2,2-trifluoroacetic acidHCID 86646237128%

Reaction Steps

To a solution of 4-(4-fluoro-phenyl)-4-[(S)-1-(4-fluoro-phenyl)-ethylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester (735 mg, 1.653 mmol) in dichloromethane (8 mL) at 0° C. was added slowly trifluoroacetic acid (1.78 mL, 23.148 mmol) and stirring continued for 12 h at room temperature. The solvent was removed under reduced pressure. Toluene was added to the residue and evaporated under reduced pressure which was repeated two times. The residue was dried under high vacuum to yield 970 mg 4-(4-fluoro-phenyl)-piperidine-4-carboxylic acid [(S)-1-(4-fluoro-phenyl)-ethyl]-amide; compound with trifluoro-acetic acid. MS ISP (m/e): 345.3 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324250B2
Source datasetuspto-grants-2012_12
ORD IDord-144ca213ab544457ace41645d71840df
Source noteuspto-grants-2012_12