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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647825Generated: October 30, 2026

1-Benzyl-N-(2-nitrocyclohexyl)piperidin-4-amine → N~1~-(1-Benzylpiperidin-4-yl)cyclohexane-1,2-diamine

https://huagongshe.com/reaction/647825

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-N-(2-nitrocyclohexyl)piperidin-4-amineHCID 13211792—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductN~1~-(1-Benzylpiperidin-4-yl)cyclohexane-1,2-diamineHCID 1321179398.3%

Reaction Steps

In this reference example, 1.0 g of 1-benzyl-4-(2-nitro-cyclohexylamino)-piperidine obtained in Reference Example 16 is dissolved in 25 ml of ethanol. Then, 1.0 g of a Raney-nickel catalyst is added thereto and the mixture is stirred at room temperature in the atmosphere of hydrogen under the atmospheric pressure. The stirring is ceased when the solution has absorbed the theoretical amount of hydrogen, and the reaction solution is filtered. The filtrate is concentrated. Consequently, 0.89 g of 1-benzyl-4-(2-aminocyclohexylamino)-piperidine is obtained as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04410528
Source datasetuspto-grants-1983_10
ORD IDord-70b95b8969a24b6c873cfaa91cd43e27
Source noteuspto-grants-1983_10