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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090691Generated: October 30, 2026

Ethyl chloroformate → ethyl N-(1-benzylpiperidin-4-yl)carbamate

https://huagongshe.com/reaction/1090691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
SolventPyridineHCID 1049—
Productethyl N-(1-benzylpiperidin-4-yl)carbamateHCID 1264184562.1%

Reaction Steps

Ethyl chloroformate (30 g, 0.276 mol) was added at 0° C. to 4-amino-1-phenylmethylpiperidine (50 g, 0.262 mol) in pyridine (600 mL). After the addition, the mixture was kept at room temperature overnight, and the pyridine was then evaporated. The residue was extracted with methylene chloride; and the resulting solution washed with water, dried over sodium sulfate, and the methylene chloride evaporated to dryness. The residue was dissolved in diisopropyl ether. A white product precipitated, which was isolated by filtration to yield 42.71 g (62%) of ethyl (1-phenylmethyl-4-piperidyl)-carbamate, m.p. 100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082847
Source datasetuspto-grants-1992_01
ORD IDord-0fe390e75e8e454c8ded6931d2c958fc
Source noteuspto-grants-1992_01