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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087094Generated: November 2, 2026

Sodium Hydroxide → 5-(Aminomethyl)-2-chloropyridine

https://huagongshe.com/reaction/1087094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5-(chloromethyl)pyridineHCID 155479—
ReactantAzane;hydrateHCID 12896473—
SolventAcetonitrileHCID 6342—
Product5-(Aminomethyl)-2-chloropyridineHCID 702092758.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 14.99g of 2-chloro-5-(chloromethyl) pyridine, 63.01g of 25% ammonia water and 60ml of acetonitrile in a stainless steel autoclave was stirred for 2 hours in an oil bath of 80° C. After adding 12.3g of 30% sodium hydroxide aqueous solution, the reaction mixture was concentrated. The residue to which 200ml of ethanol were added was dried over anhydrous magnesium sulfate and, filtered to remove insoluble materials. The filtrate was concentrated and purified by a column chromatography [developing solvent: dichloromethane-methanol (4:1)] to afford 7.66g of 5-(aminomethyl)-2- chloropyridine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034404
Source datasetuspto-grants-1991_07
ORD IDord-42613b3047a549fe8e068f616e772585
Source noteuspto-grants-1991_07