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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49779Generated: October 26, 2026

Water → 1-Acetyl-4-(4-fluorophenoxycarbonylamino)piperidine

https://huagongshe.com/reaction/49779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant4-Fluorophenyl chloroformateHCID 2733256—
Reactant1-Acetyl-4-aminopiperidine hydrochlorideHCID 17221642—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-Acetyl-4-(4-fluorophenoxycarbonylamino)piperidineHCID 9817161—

Reaction Steps

To a suspension of 1-acetyl-4-aminopiperidine hydrochloride (0.4 g) in dichloromethane (5 ml) were added in turn pyridine (0.54 ml) and 4-fluorophenyl chloroformate (0.29 ml) at 0° C. The mixture was allowed to warm to ambient temperature and stirred for 1 hour, which was taken up into a mixture of water and ethyl acetate. The separated organic layer was washed in turn with hydrochloric acid (1N), aqueous sodium hydrogen carbonate, and brine, and dried over magnesium sulfate. Evaporation under reduced pressure gave a residue, which was triturated with diisopropyl ether to give 1-acetyl-4-(4-fluorophenoxycarbonylamino)piperidine (347 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710043B1
Source datasetuspto-grants-2004_03
ORD IDord-e12882cfc33742e9af733bf1dc0f1f80
Source noteuspto-grants-2004_03