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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650968Generated: October 27, 2026

Triethylamine → 1-Benzyloxycarbonyl-3-piperidone

https://huagongshe.com/reaction/650968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantPiperidin-3-oneHCID 33722—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-Benzyloxycarbonyl-3-piperidoneHCID 1514169—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-piperidone (12 mmol) in 200 mL of methylene chloride. is added triethylamine (18 mmol) in a single portion at room temperature and the reaction mixture cooled to 0° C. Benzyl chloroformate (12 mmol) is added dropwise via addition funnel and the reaction mixture allowed to warm to room temperature. Stirring is continued for 2 hours at room temperature. The reaction mixture is diluted with ethyl acetate (200 mL) and washed with 1N hydrochloric acid (3×100 mL), water and brine. The organic layer is worked up to provide N-Benzyloxycarbonyl-3-piperidone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277865B1
Source datasetuspto-grants-2001_08
ORD IDord-b80596e8795847d2a8083ccfffd02bdf
Source noteuspto-grants-2001_08