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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239749Generated: October 28, 2026

Acetyl chloride → (S)-5-aminopiperidin-2-one hydrochloride

https://huagongshe.com/reaction/2239749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
Reactant(S)-tert-butyl 6-oxopiperidin-3-ylcarbamateHCID 15466433—
SolventEthanolHCID 702—
Product(S)-5-aminopiperidin-2-one hydrochlorideHCID 4261451899%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-((3S)-6-Oxo(3-piperidyl))(tert-butoxy)carboxamide (3.9 mmol, 0.83 g) were dissolved in ethanol (10 mL) and cooled to 0° C. Acetyl chloride (2 mL) was added and the reaction was allowed to reach room temperature. The reaction was stirred for 1 hour after which the solvent was removed in vacuo to yield the title compound (725 mg, 99% yield) as the dihydrochloride salt. ES-MS: 115 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723340B2
Source datasetuspto-grants-2010_05
ORD IDord-378afabc157941deb50e0323369a44f3
Source noteuspto-grants-2010_05