Chloropyridine
| Related molecular formulas | ||
|---|---|---|
| C5H6ClN | ||
| C4H2ClN | C5H4ClN | C6H6ClN |
| C5H2ClN | ||
| C5H3Cl | C5H5ClN2 | |
Chloropyridines are a group of aryl chlorides consisting of a pyridine ring with chlorine atoms as substituents.
Chloropyridines include:
Production
[edit]
Direct halogenation of pyridine with chlorine gas above 270 °C gives a mixture of 2-chloropyridine and 2,6-dichloropyridine.[1]
2- and 4-chloropyridine are prepared from the corresponding pyridinols using phosphoryl chloride.[1]
Uses
[edit]Chloropyridines are important intermediates to pharmaceuticals and agrochemicals.[1] A major use of 2-chloropyridine is the production of production of the fungicide pyrithione. Reaction of 4-chloropyridine with thioglycolic acid gives pyridylmercaptoacetic acid, a step in the production of cephalosporin antibiotics.
See also
[edit]References
[edit]- 1 2 3 Siegemund, Günter; Schwertfeger, Werner; Feiring, Andrew; Smart, Bruce; Behr, Fred; Vogel, Herward; McKusick, Blaine (2000). "Pyridine and Pyridine Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a22_399. ISBN 978-3-527-30673-2.
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