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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565982Generated: October 29, 2026

2-(4-Nitrobenzyl)pyridine → 2-(4-Aminobenzyl)pyridine

https://huagongshe.com/reaction/565982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Nitrobenzyl)pyridineHCID 69292—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(4-Aminobenzyl)pyridineHCID 45952584.5%

Reaction Steps

A mixture of 2-(4-nitrobenzyl)pyridine (J. Chem. Soc., p549, 1929) (1.50 g) and 5% Pd-C (0.15 g) in ethanol (30 ml) was vigorously stirred under hydrogen atmosphere for 8 hours, and the Pd-C was filtered off. The filtrate was concentrated under reduced pressure, and the residue was separated and purified with column chromatography (ethyl acetate/hexane=1:1→2:1) to give 2-(4-aminobenzyl)-pyridine (1.09 g) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-1d08ebd1338b44aba9b58dffaee7fb23
Source noteuspto-grants-2001_01