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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334859Generated: October 31, 2026

tert-Butyl [(3S,5S)-5-(2-fluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)piperidin-3-yl]carbamate → (3S,5S)-3-amino-5-(2-fluorophenyl)-1-(2,2,2-trifluoroethyl)piperidin-2-one

https://huagongshe.com/reaction/334859

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl [(3S,5S)-5-(2-fluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)piperidin-3-yl]carbamateHCID 86707239—
SolventEthyl AcetateHCID 8857—
Product(3S,5S)-3-amino-5-(2-fluorophenyl)-1-(2,2,2-trifluoroethyl)piperidin-2-oneHCID 68358316—

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of tert-butyl[(3S,5S)-5-(2-fluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)piperidin-3-yl]carbamate (126 mg, 0.32 mmol) in ethyl acetate (10 mL), pre-cooled to 0° C. was sparged with HCl gas for ˜1 min. The ice-bath was removed and the acidic solution was allowed to warm to 23° C. as stirring was continued for 2 h. The mixture was then concentrated to dryness to afford the title compound as a hydrochloride salt. MS: m/z=291.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883807B2
Source datasetuspto-grants-2014_11
ORD IDord-6833cfc2ea3a4ce884e423db53beea98
Source noteuspto-grants-2014_11