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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803216Generated: November 1, 2026

Trifluoroacetic acid → 1-Amino-6-(4-fluorophenyl)piperidin-2-one

https://huagongshe.com/reaction/1803216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 2-(4-fluorophenyl)-6-oxopiperidin-1-ylcarbamateHCID 66859411—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-Amino-6-(4-fluorophenyl)piperidin-2-oneHCID 5811012890%

Reaction Steps

Step AAG (3): To a soln of tert-butyl 2-(4-fluorophenyl)-6-oxopiperidin-1-ylcarbamate (330 mg, 1.07 mmol) in CH2Cl2 (5 mL) was added TFA (1.00 mL, 13.0 mmol). The mixture was stirred at for 2 hrs. The solvent was removed in vacuo. The crude reaction was diluted with EtOAc (100 mL). The organic layer was separated and washed with saturated aqueous NaHCO3 solution, dried over Na2SO4, filtered, and concentrated in vacuo to afford 1-amino-6-(4-fluorophenyl)piperidin-2-one (200 mg, 90% yield). LC-MS (M+H)+ 209.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349880B2
Source datasetuspto-grants-2013_01
ORD IDord-f701bac0489543e08125eb6b6730117d
Source noteuspto-grants-2013_01