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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54553Generated: October 25, 2026

(E)-3-(1-benzylpiperidin-4-yl)-2-propenenitrile → 3-(1-Benzylpiperidin-4-yl)propanenitrile

https://huagongshe.com/reaction/54553

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-3-(1-benzylpiperidin-4-yl)-2-propenenitrileHCID 19959219—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
Product3-(1-Benzylpiperidin-4-yl)propanenitrileHCID 1995925648.7%

Reaction Steps

A mixture of (E)-3-(1-benzylpiperidin-4-yl)-2-propenenitrile (5.5 g) and platinum(IV) oxide (0.5 g) in methanol (70 ml) was hydrogenated at atmospheric pressure for 8 hours. After platinum(IV) oxide was removed by filtration, the filtrate was evaporated in vacuo to give 3-(1-benzylpiperidin-4-yl)propanenitrile (2.7 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622976
Source datasetuspto-grants-1997_04
ORD IDord-fbff4cd895f240f5b72f30be0cb0df21
Source noteuspto-grants-1997_04