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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154706Generated: October 26, 2026

3-[(4-Nitrophenyl)methyl]pyridine → 4-(Pyridin-3-ylmethyl)aniline

https://huagongshe.com/reaction/1154706

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(4-Nitrophenyl)methyl]pyridineHCID 13364860—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(Pyridin-3-ylmethyl)anilineHCID 10375133—

Reaction Steps

A solution of 3-(4'-nitrobenzyl)pyridine of Preparation 7 (7.924 g, 0.0370 mole) in methanol (100 ml) is shaken with 5% Pd on carbon and hydrogen in a Parr apparatus. Hydrogen uptake is complete within 45 min. The catalyst is removed by filtration through sintered glass. The solvent is removed under reduced pressure. The crystalline residue is recrystallized from methylene chloride-hexane with a first crop of 5.229 g; a second crop of 0.492 g; a third crop of 0.480 g; and a fourth crop of 0.137 g (total 6.338 g, 0.0347 mole, 94%). Recrystallization from CH2Cl2 -hexane gives colorless crystals of the titled product with a melting point of 121°-123° C.; IR (nujol) peaks are observed at 3400, 3300, 3200, 1640, 1610, 1590, 1575, 1515, 1480, 845, 800, and 710 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490531
Source datasetuspto-grants-1984_12
ORD IDord-e898bcc67cb246b196d02ebff631d102
Source noteuspto-grants-1984_12