HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088381Generated: October 26, 2026
1-Phenethylamine → (+)-Ethyl cis-3-methoxy-4-[(1-phenylethyl)amino]-1-piperidinecarboxylate
https://huagongshe.com/reaction/1088381
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenethylamine | HCID 7408 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Ethyl 3-methoxy-4-oxopiperidine-1-carboxylate | HCID 2724451 | — |
| Reactant | 1-[4-(chloromethyl)phenyl]-1H-imidazole hydrochloride | HCID 19794662 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (+)-Ethyl cis-3-methoxy-4-[(1-phenylethyl)amino]-1-piperidinecarboxylate | HCID 67914576 | 51% |
Reaction Steps
A solution of 20 parts of ethyl 3-methoxy-4-oxo-1-piperidinecarboxylate, 12 parts of (-)-α-methylbenzenemethanamine, 2 parts of a solution of thiophene in ethanol 4% and 200 parts of methanol was hydrogenated at normal pressure and at room temperature with 4 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated in vacuo. The residue was purified by HPLC using a mixture of hexane, trichloromethane and methanol (50:49.5:0.5 by volume) as eluent. The pure A-fractions were collected and the eluent was evaporated, yielding 15.62 parts (51%) of (-)-ethyl cis-3-methoxy-4-[(1-phenylethyl)-amino]-1-piperidinecarboxylate as a residue (intermediate 103).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04962115 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-41652eba5e184a67a8ef820904ebaec3 |
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| Source note | uspto-grants-1990_10 |
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