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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-(3-Methylphenyl)-2-[1-(phenylmethyl)-4-piperidinyl]ethanone | HCID 20288047 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-[2-(3-methylphenyl)-2-oxoethyl]-1-piperidinecarboxylate | HCID 20288050 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04254127 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-e00cb53976ae4c9ea04bb7d19aeff99b |
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| Source note | uspto-grants-1981_03 |
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