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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387764Generated: October 31, 2026

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

https://huagongshe.com/reaction/1387764

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 numberUS06268354B1
Source datasetuspto-grants-2001_07
ORD IDord-1e282cdf0424491f98045e5eb2d0dd0e
Source noteuspto-grants-2001_07