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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantEthyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylateHCID 12414163—
SolventEthanolHCID 702—
ProductEthyl trans-3-hydroxy-4-[(phenylmethyl)amino]-1-piperidinecarboxylateHCID 13677850—
ProductEthyl trans-4-hydroxy-3-[(phenylmethyl)amino]-1-piperidinecarboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057525
Source datasetuspto-grants-1991_10
ORD IDord-7e65da6c0a2e4c6e8112a9f63e6911ff
Source noteuspto-grants-1991_10