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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814851Generated: November 2, 2026

Ethyl chloroformate → Ethyl 3-methyl-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/1814851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
SolventBenzeneHCID 241—
ProductEthyl 3-methyl-4-oxopiperidine-1-carboxylateHCID 15075657—

Reaction Steps

Ethyl chloroformate (3.0 g, 26.7 mmol) was added to a stirred solution of 1-benzyl-3-methyl-4-piperidinone (2.0 g, 9.85 mmol) in benzene (30 ml) at ambient temperature. The obtained reaction mixture was refluxed with stirring for 6 hr and concentrated to dryness to give 1-carbethoxy-3-methyl-4-piperidone as oil. Yield 1.4 g (77%), C9H15NO3, m/z 186 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878713B2
Source datasetuspto-grants-2005_04
ORD IDord-ad6a2bae7782438baf0d42171f0e1230
Source noteuspto-grants-2005_04