Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165040Generated: October 31, 2026

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

https://huagongshe.com/reaction/1165040

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 numberUS04906643
Source datasetuspto-grants-1990_03
ORD IDord-495c9733dcaf4ee1803f1c0cb4d09dfc
Source noteuspto-grants-1990_03