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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565831Generated: October 25, 2026

1-(4-Nitrobenzyl)piperidine → 4-(Piperidin-1-ylmethyl)aniline

https://huagongshe.com/reaction/565831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Nitrobenzyl)piperidineHCID 783541—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(Piperidin-1-ylmethyl)anilineHCID 84615018.2%

Reaction Steps

In ethanol (50 ml) was dissolved 1-(4-nitrobenzyl)piperidine (6.41 g), and 10% dried palladium on carbon (0.33 g) was added to the mixture. Under hydrogen atmosphere, the mixture was stirred at room temperature under atmospheric pressure for 24 hours. The palladium was filtered off, and the filtrate was concentrated. The residue was recrystallized from hexane to give 1-(4-aminobenzyl)piperidine (1.01 g) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-503b4ff6a8fa4e7798c018ced35f5f00
Source noteuspto-grants-2001_01