2-chloropyridine
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Preferred IUPAC name
2-Chloropyridine
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3D model (Jmol)
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| ECHA InfoCard | 100.003.316 | ||
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| Properties | |||
| C5H4ClN | |||
| Molar mass | 113.54 g/mol | ||
| Appearance | colorless liquid | ||
| Melting point | −46 °C (−51 °F; 227 K) | ||
| Boiling point | 166 °C (331 °F; 439 K) | ||
| 27 g/L | |||
| Acidity (pKa) | 0.49 | ||
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| Safety data sheet | MSDS | ||
| R-phrases | R23 R38 | ||
| S-phrases | S26 S37 S39 S45 | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2-Chloropyridine is an organohalide 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.
2-Choropyridine was originally described in 1898 by the chlorination of 2-hydroxypyridine. A typical chlorinating agent is phosphoryl chloride. It can also be generated by halogenating pyridine. This reaction affords a mixture of 2-chloro and 2,6-dichloropyridine.
Alternatively, 2-chloropyridines can be conveniently synthesized in high yields from pyridine-N-oxides.
2-Chloropyridine reacts with nucleophiles to generate pyridine derivatives substituted at the second and fourth carbons on the heterocycle. Therefore, many reactions using 2-chloropyridine generate mixtures of products which require further workup to isolate the desired isomer.
2-chloropyridine is primarily used to generate other pyridine derivatives. Some commercial products include pyrithione, pyripropoxyfen, chlorphenamine, and disopyramide. These reactions rely on chloride’s nature as a good leaving group to facilitate the transfer of a substrate onto the pyridine ring. Pyrithione, the conjugate base of 2-mercaptopyridine-N-oxide, is a fungicide found in some shampoos. It is generated from 2-chloropyridine by reacting the N-oxide of 2-chloropyridine with Na2S in a basic solution, before adding aqueous HCl. Used as an antihistamine, pheniramine may be generated via several different pathways. One synthesis is to hydroformylate functionalized olefins. This reaction proceeds by reacting phenylacetonitrile with 2-chloropyridine in the presence of a base. The resulting intermediate is then alkylated by 2-(dimethylamino)ethyl chloride and the cyano group removed.
Though 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.
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