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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091060Generated: November 3, 2026

Ammonia → 5-(Aminomethyl)-2-chloropyridine

https://huagongshe.com/reaction/1091060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAcetonitrileHCID 6342—
Reactant2-Chloro-5-(chloromethyl)pyridineHCID 155479—
SolventSodium HydroxideHCID 14798—
Product5-(Aminomethyl)-2-chloropyridineHCID 7020927—

Reaction Conditions

Temperature80 °C

Reaction Steps

A stainless steel autoclave was charged with 14.99 g of 2-chloro-5-(chloromethyl)pyridine, 63.01 g of 25% aqueous ammonia and 60 ml of acetonitrile and the mixture was stirred on an oil bath at 80° C. for 2 hours. The reaction mixture was diluted with 12.3 g of 30% aqueous sodium hydroxide solution and concentrated. The residue was diluted with 200 ml of ethanol, dried over anhydrous magnesium sulfate and filtered to remove the insolubles. Finally, the filtrate was concentrated and purified by column chromatography (eluent: dichloromethane-methanol (4:1)) to give 7.66 g of 5-(aminomethyl)-2-chloropyridine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05084459
Source datasetuspto-grants-1992_01
ORD IDord-fa4336e9719248078117ba88a3c19bea
Source noteuspto-grants-1992_01