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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280787Generated: October 27, 2026

4-(1-Benzylpiperidin-3-yliden)-butyronitrile → 4-(1-Benzylpiperidin-3-ylidene)-butylamine

https://huagongshe.com/reaction/1280787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-Benzylpiperidin-3-yliden)-butyronitrileHCID 53987194—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product4-(1-Benzylpiperidin-3-ylidene)-butylamineHCID 70159544—

Reaction Steps

8.0 g (33.3 mmol) 4-(1-benzylpiperidin-3-ylidene)-butyronitrile are dissolved in 80 ml ethanol and added to a spatula tip of Raney-Nickel. The mixture is stirred under hydrogen atmosphere until consumption of the theoretical amount of hydrogen to be taken up (ca. 5 days). The mixture is filtered from the catalyst and the solvent is removed under vacuum. The residue is chromatographically purified Voice over silica gel with CHCl3/CH3OH/NH4OH (90/10/1). After drawing off the solvent, a colorless oil remains which is further processed without additional purification. Yield. 3.9 g (47%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451816B1
Source datasetuspto-grants-2002_09
ORD IDord-7c05bd4657534792bcff8dc8480c28f0
Source noteuspto-grants-2002_09