2-Chloropyridine


2-Chloropyridine is an aryl chloride with the formula C5H4ClN. It is a colorless liquid that is mainly used to generate fungicides and insecticides in industry. It also serves to generate antihistamines and antiarrythymics for pharmaceutical purposes. It is one of three isomers of chloropyridine.

Preparation

2-Chloropyridine is produced by direct reaction of pyridine with chlorine. The initially formed 2-chloropyridine reacts further to give 2,6-dichloropyridine.
Alternatively, 2-chloropyridines can be conveniently synthesized in high yields from pyridine-N-oxides.
2-Chloropyridine was originally prepared by the chlorination of 2-hydroxypyridine with phosphoryl chloride.

Main reactions and applications

2-Chloropyridine undergoes substitution at the C-Cl bond. Some reactions using 2-chloropyridine generate mixtures of products.
Some commercial products include pyrithione, pyripropoxyfen, chlorphenamine, and disopyramide. In these conversions, chloride is displaced. Pyrithione, the conjugate base of 2-mercaptopyridine-N-oxide, is a fungicide found in some shampoos. Oxidation 2-chloropyridine gives 2-chloropyridine-N-oxide. The antihistamine pheniramine may be generated via the reaction of phenylacetonitrile with 2-chloropyridine in the presence of a base.

Environmental properties

Although pyridine is an excellent source of carbon, nitrogen, and energy for certain microorganisms, introduction of a halogen moiety significantly retards degradation of the pyridine ring. With the exception of 4-chloropyridine, each of the mono- and di-substituted chloropyridines were found to be relatively resistant to microbiological degradation in soil or liquid media. Estimated time for complete degradation was > 30 days. 2-Chloropyridine exhibits extensive volatilization losses from water, less so when present in soil.

Toxicity

The is 64 mg/kg.