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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654174Generated: October 30, 2026

Ammonia → trans-1-(2-Aminoethyl)-4-[(phenylmethyl)amino]-3-piperidinol

https://huagongshe.com/reaction/654174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactanttrans-3-Hydroxy-4-[(phenylmethyl)amino]-1-piperidineacetonitrileHCID 14854945—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Producttrans-1-(2-Aminoethyl)-4-[(phenylmethyl)amino]-3-piperidinolHCID 6783356091.6%

Reaction Steps

A mixture of 12 parts of trans-3-hydroxy-4-[(phenylmethyl)amino]-1-piperidineacetonitrile and 320 parts of methanol, saturated with ammonia was hydrogenated at normal pressure and at room temperature with 3 parts of Raney-nickel catalyst. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated to dry, yielding 11.2 parts (91.6%) of trans-1-(2-aminoethyl)-4-[(phenylmethyl)amino]-3-piperidinol as a residue (interm. 17).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05130312
Source datasetuspto-grants-1992_07
ORD IDord-ae58485c610040b1aa0f126c234753b0
Source noteuspto-grants-1992_07