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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512979Generated: November 3, 2026

Ethyl Acetate → 5-Amino-4-methylpyridine-2-carbonitrile

https://huagongshe.com/reaction/1512979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Methyl-5-nitropyridine-2-carbonitrileHCID 23000171—
CatalystZincHCID 23994—
SolventWaterHCID 962—
Product5-Amino-4-methylpyridine-2-carbonitrileHCID 5528982146.1%

Reaction Steps

To a suspension of 2-cyano-4-methyl-5-nitropyridine (1.86 g) and ammonium chloride (3.05 g) in water (50 mL) was added zinc (7.46 g) under ice-cooling over 10 minutes, and the mixture was stirred at the same temperature for 1 hour. To the reaction mixture was added ethyl acetate (50 mL), and the resulting mixture was stirred at room temperature for 30 minutes. The insoluble material was removed by filtration, and the organic layer of the filtrate was separated. The organic layer was washed with brine, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residual solids were suspended in a mixed solvent (n-hexane/ethyl acetate=1/1), and collected by filtration. The collected solids were dried under reduced pressure to give the title compound (0.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217069B2
Source datasetuspto-grants-2012_07
ORD IDord-42cc8d3c11264404811a0f8d1496e31c
Source noteuspto-grants-2012_07