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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126863Generated: October 26, 2026

Chloroform → Ethyl 4-[2-(3-methylphenyl)-2-oxoethyl]-1-piperidinecarboxylate

https://huagongshe.com/reaction/126863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl chloroformateHCID 10928—
Reactant1-(3-Methylphenyl)-2-[1-(phenylmethyl)-4-piperidinyl]ethanoneHCID 20288047—
SolventWaterHCID 962—
ProductEthyl 4-[2-(3-methylphenyl)-2-oxoethyl]-1-piperidinecarboxylateHCID 2028805091%

Reaction Steps

To a stirred mixture of 20.9 parts of 1-(3-methylphenyl)-2-[1-(phenylmethyl)-4-piperidinyl]ethanone, 0.75 parts of sodium carbonate and 150 parts of trichloromethane are added dropwise 8.1 parts of ethyl chloroformate. Upon completion, stirring is continued overnight at room temperature. Water is added to the reaction mixture and the layers are separated. The aqueous phase is extracted with trichloromethane. The combined organic phases are washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 18 parts (91%) of ethyl 4-[2-(3-methylphenyl)-2-oxoethyl]-1-piperidinecarboxylate as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254127
Source datasetuspto-grants-1981_03
ORD IDord-e00cb53976ae4c9ea04bb7d19aeff99b
Source noteuspto-grants-1981_03