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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486436Generated: October 26, 2026

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

https://huagongshe.com/reaction/486436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
SolventTolueneHCID 1140—
ProductEthyl 3-methyl-4-oxopiperidine-1-carboxylateHCID 1507565783%

Reaction Steps

To a stirred solution of 152 parts of 3-methyl-1-(phenylmethyl)-4-piperidinone in 900 parts of methylbenzene were added dropwise 218 parts of ethyl carbonochloridate at room temperature. Upon completion, stirring was continued overnight at reflux. After cooling, the reaction mixture was washed with water and hydrochloric acid, dried, filtered and evaporated. The residue was distilled, yielding 120.5 parts (83%) of ethyl 3-methyl-4-oxo-1-piperidinecarboxylate; bp. 98°-105° C. at 1 mm pressure (intermediate 26).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292738
Source datasetuspto-grants-1994_03
ORD IDord-abcf0f1d31534ab2b8f0fd36767139f3
Source noteuspto-grants-1994_03