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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54554Generated: October 27, 2026

Ammonium Hydroxide → 3-(1-Benzylpiperidin-4-yl)propan-1-amine

https://huagongshe.com/reaction/54554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant3-(1-Benzylpiperidin-4-yl)propanenitrileHCID 19959256—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product3-(1-Benzylpiperidin-4-yl)propan-1-amineHCID 1995920578.6%

Reaction Steps

A mixture of 3-(1-benzylpiperidin-4-yl)propanenitrile (0.5 g), Raney nickel (0.3 ml) and a conc. ammonia aqueous solution (1 ml) in ethanol (10 ml) was hydrogenated at atmospheric pressure for 6 hours. After Raney nickel was removed by filtration, the filtrate was evaporated in vacuo. The residue was chromatographed on alumina eluting with 2% methanol in chloroform and the fractions containing the object product were collected and evaporated to give 3-(1-benzylpiperidin-4-yl)propylamine (0.4 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622976
Source datasetuspto-grants-1997_04
ORD IDord-b684a9927b4f4434827faf834b653fd7
Source noteuspto-grants-1997_04