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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833371Generated: November 1, 2026

Ethylene Oxide → Ethyl 1-(2-hydroxyethyl)-4-phenylpiperidine-4-carboxylate

https://huagongshe.com/reaction/1833371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
ReactantMethyl Isobutyl KetoneHCID 7909—
ReactantNormeperidineHCID 32414—
SolventEthanolHCID 702—
ProductEthyl 1-(2-hydroxyethyl)-4-phenylpiperidine-4-carboxylateHCID 21389218—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 9.9 parts of ethyl 4-phenyl-4-piperidinecarboxylate, 41.8 parts of 4-methyl-2-pentanone, 4.3 parts of ethylene oxide and 79.2 parts of ethanol is heated in a sealed citric bottle at about 60° C for 7 days. The resulting solution is cooled, the solvent is evaporated under reduced pressure and the residual material is partitioned between diluted NaOH and ether. The ether layer is then separated and extracted with diluted HCl. The acid layer is then made alkaline with aqueous sodium hydroxide and the resulting mixture is extracted with ether. The ether layer is dried over sodium sulfate and potassium carbonate and evaporated in vacuum. The residue is crystallized from ether-n-pentane to give ethyl 1-(2-hydroxyethyl)-4-phenyl-4-piperidinecarboxylate, melting at about 91.5°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066654
Source datasetuspto-grants-1978_01
ORD IDord-b360bb82430c4fa9b93e45c9d5d136a4
Source noteuspto-grants-1978_01