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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Normeperidine | HCID 32414 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1-(2-hydroxyethyl)-4-phenylpiperidine-4-carboxylate | HCID 21389218 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04066654 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-b360bb82430c4fa9b93e45c9d5d136a4 |
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| Source note | uspto-grants-1978_01 |
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