HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345539Generated: October 29, 2026
Benzylamine → Ethyl trans-3-hydroxy-4-[(phenylmethyl)amino]-1-piperidinecarboxylate
https://huagongshe.com/reaction/345539
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Ethyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate | HCID 12414163 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl trans-3-hydroxy-4-[(phenylmethyl)amino]-1-piperidinecarboxylate | HCID 13677850 | — |
| Product | Ethyl trans-4-hydroxy-3-[(phenylmethyl)amino]-1-piperidinecarboxylate | HCID 67312643 | — |
Reaction Steps
A mixture of 3.4 parts of ethyl 7-oxa-3-azabicyclo[4,1,0]heptane-3-carboxylate, 2.1 parts of benzenemethanamine and 40 parts of ethanol was stirred and refluxed for 17 hours. Another 0.3 parts of ethyl 7-oxa-3-azabicyclo[4,1,0]heptane-3-carboxylate were added and stirring at reflux was continued for 4 hours. The reaction mixture was evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 3.4 parts (61.8%) of a mixture of ethyl trans-3-hydroxy-4-[(phenylmethyl)amino]-1-piperidinecarboxylate and ethyl trans-4-hydroxy-3-[(phenylmethyl)amino]-1-piperidinecarboxylate as an oily residue (intermediate 35 and 36).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057525 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-7e65da6c0a2e4c6e8112a9f63e6911ff |
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| Source note | uspto-grants-1991_10 |
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