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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075452Generated: November 1, 2026

2-(3-Nitrophenyl)pyridine → 3-(2-Pyridyl)aniline

https://huagongshe.com/reaction/1075452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Nitrophenyl)pyridineHCID 459555—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(2-Pyridyl)anilineHCID 45951788%

Reaction Steps

To a solution of 2-(3-nitrophenyl)pyridine (prepared as described in J. Chem. Soc. 1958 p. 1759) (12.7g, 63.5mmol) in abs. ethanol is added palladium catalyst (1.3g 5% Pd on activated carbon) and the mixture is hydrogenated at ambient pressure until the hydrogen uptake has ceased. The mixture is filtered through celite and the filtrate is concentrated under reduced pressure. The residue is purified by column-chromatography on silica gel using a mixture of ethyl acetate and petroleum ether (9:1)as the eluent to afford 2f (9.5g, 88%) as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05902813
Source datasetuspto-grants-1999_05
ORD IDord-daaf52169366414483f2601633266ee4
Source noteuspto-grants-1999_05