2-Chloropyridine
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| Names | |||
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| Preferred IUPAC name
2-Chloropyridine | |||
| Identifiers | |||
3D model (JSmol) |
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| 105788 | |||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.003.316 | ||
| EC Number |
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| 130818 | |||
PubChem CID |
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| RTECS number |
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| UNII | |||
| UN number | 2822 | ||
CompTox Dashboard (EPA) |
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| Properties | |||
| C5H4ClN | |||
| Molar mass | 113.54 g·mol−1 | ||
| Appearance | colorless liquid | ||
| Density | 1.2 g/mL | ||
| Melting point | −46 °C (−51 °F; 227 K) | ||
| Boiling point | 166 °C (331 °F; 439 K) | ||
| 27 g/L | |||
| Acidity (pKa) | 0.49 (for C5H4ClNH+) [1] | ||
| Hazards | |||
| GHS labelling: | |||
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| Danger | |||
| H301, H310, H315, H319, H330, H400 | |||
| P260, P262, P264, P270, P271, P273, P280, P284, P301+P310, P301+P312, P302+P350, P302+P352, P304+P340, P305+P351+P338, P310, P311, P312, P314, P320, P321, P330, P332+P313, P337+P313, P361, P362, P363, P391, P403+P233, P405, P501 | |||
| Safety data sheet (SDS) | MSDS | ||
| Related compounds | |||
Related compounds |
3-Chloropyridine 3-Bromopyridine 2-Chloromethylpyridine | ||
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 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.[2] It is one of three isomers of chloropyridine.
Preparation
[edit]
2-Chloropyridine is produced by direct reaction of pyridine with chlorine. The initially formed 2-chloropyridine reacts further to give 2,6-dichloropyridine.[2]
Alternatively, 2-chloropyridines can be conveniently synthesized in high yields from pyridine-N-oxides.[3]
2-Chloropyridine was originally prepared by the chlorination of 2-hydroxypyridine with phosphoryl chloride.[4]
Main reactions and applications
[edit]2-Chloropyridine undergoes substitution at the C-Cl bond.[5][6] Some reactions using 2-chloropyridine generate mixtures of products.[2]
Some commercial products include pyrithione, pyripropoxyfen, chlorphenamine, and disopyramide. In these conversions, chloride is displaced.[2] Pyrithione, the conjugate base of 2-mercaptopyridine-N-oxide, is a fungicide found in some shampoos. Oxidation 2-chloropyridine gives 2-chloropyridine-N-oxide.[7] The antihistamine pheniramine may be generated via the reaction of phenylacetonitrile with 2-chloropyridine in the presence of a base.[8]
Environmental properties
[edit]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.[9] Estimated time for complete degradation was > 30 days. 2-Chloropyridine exhibits extensive volatilization losses from water, less so when present in soil.[10]
Toxicity
[edit]References
[edit]- ↑ Linnell, Robert (1960). "Notes- Dissociation Constants of 2-Substituted Pyridines". The Journal of Organic Chemistry. 25 (2): 290. doi:10.1021/jo01072a623.
- 1 2 3 4 5 Shimizu, Shinkichi; Watanabe, Nanao; Kataoka, Toshiaki; Shoji, Takayuki; Abe, Nobuyuki; Morishita, Sinji; Ichimura, Hisao (2007). "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.
- ↑ Narendar, P.; Gangadasu, B.; Ramesh, Ch.; China Raju, B.; Jayathirtha Rao, V. (2004). "Facile and Selective Synthesis of Chloromethylpyridines and Chloropyridines Using Diphosgene/Triphosgene". Synthetic Communications. 34 (6): 1097–1103. doi:10.1081/SCC-120028642. S2CID 95706122.
- ↑ Pechmann, H. V.; Baltzer, O. (1891). "Ueber das α-Pyridon (α-Oxypyridin)". Berichte der Deutschen Chemischen Gesellschaft. 24 (2): 3144–3153. doi:10.1002/cber.189102402155.
- ↑ Kevin W. C. Poon, Philip A. Albiniak, Gregory B. Dudley (2007). "Protection of Alcohols Using 2-Benzyloxy-1-Methylpyridinium Trifluoromethanesulfonate: Methyl (R)-(-)-3-Benzyloxy-2-Methyl Propanoate". Organic Syntheses. 84: 295. doi:10.15227/orgsyn.084.0295.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ↑ Patrick M. Pollock, Kevin P. Cole (2012). "t-Butyl as a Pyrazole Protecting Group: Preparation and Use of 1-tert-Butyl-3-Methyl-1H-Pyrazole-5-Amine". Organic Syntheses. 89: 537. doi:10.15227/orgsyn.089.0537.
- ↑ Cheng, Hefeng; She, Ji. 14. Improved preparation of 2-mercaptopyridine-N-oxide. Zhongguo Yiyao Gongye Zazhi. 1990, 21, (2), pp. 55-56. ISSN 1001-8255
- ↑ Botteghi, Carlo; Chelucci, Giorgio; Del Ponte, Gino; Marchetti, Mauro; Paganelli, Stefano (1994). "New Synthetic Route to Pheniramines via Hydroformylation of Functionalyzed Olefins". The Journal of Organic Chemistry. 59 (23): 7125–7127. doi:10.1021/jo00102a044.
- ↑ Sims, G. K. and L.E. Sommers. 1986. Biodegradation of pyridine derivatives in soil suspensions. Environmental Toxicology and Chemistry. 5:503-509.
- ↑ Sims, G. K. and L.E. Sommers. 1985. Degradation of pyridine derivatives in soil. Journal of Environmental Quality. 14:580-584.