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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228173Generated: October 30, 2026

Pyridine, 2-((4-nitrophenyl)methyl)- → 2-(4-Aminobenzyl)pyridine

https://huagongshe.com/reaction/2228173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine, 2-((4-nitrophenyl)methyl)-HCID 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:→2:1) to give 2—(4-aminobenzyl)-pyridine (1.09 g) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-3fba5fbd0187442382e1dd9f1427a369
Source noteuspto-grants-2002_07