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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872064Generated: October 26, 2026

2,4,6-Trimethyl-3-nitropyridine → 2,4,6-Trimethyl-3-pyridinamine

https://huagongshe.com/reaction/1872064

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-Trimethyl-3-nitropyridineHCID 2747698—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2,4,6-Trimethyl-3-pyridinamineHCID 98846—

Reaction Steps

3-Nitro-2,4,6-trimethylpyridine (14.89 g, 89.70 mmol) in methanol (250 ml) containing 10% palladium/carbon (1.5 g) was hydrogenated at 55 psi for 2 hours. The reaction mixture was filtered through wet celite, and the celite filter rinsed with methanol (5×30 ml). The filtrate was concentrated in vacuo to dryness and the residue purified by chromatography (silica gel; methylene chloride/methanol, 95/5) to 3-amino-2,4,6-trimethylpyridine (12.42 g, 100%) as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107301
Source datasetuspto-grants-2000_08
ORD IDord-3198ed2322d8423180688cdb50cfae3e
Source noteuspto-grants-2000_08