Difference between revisions of "Azine"
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Physchim62 (talk | contribs) (→Reactions and uses) |
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==Reactions and uses== | ==Reactions and uses== | ||
| − | Azines have been used as sources of hydrazine produced ''in situ'', for example | + | Azines have been used as sources of hydrazine produced ''in situ'', for example in the production of [[herbicide]] precursor [[1,2,4-triazole]].<ref>{{citation | inventor1-last = Nagata | inventor1-first = Nobuhiro | inventor2-last = Nishizawa | inventor2-first = Chiharu | inventor3-last = Kurai | inventor3-first = Toshikiyo | assignee = Mitsubishi Gas Chemical Co. | title = Method of producing 1,2,4-triazole | country-code = US | patent-number = 6002015 | issue-date = 1999-12-14}}.</ref> |
==Nomenclature== | ==Nomenclature== | ||
Revision as of 09:06, 2 July 2010
Azines are a functional class of organic compounds, formed from the condensation reaction of two equivalents of an aldehyde or ketone with one equivalent of hydrazine.[1][2] They may be further classified as aldazines or ketazines, depending on the nature of the carbonyl compound.[3][4]
Preparation
Azines may be prepared by the direct reaction of a carbonyl compound with hydrazine hydrate:[5] the reaction is exothermic.[6]
Reactions and uses
Azines have been used as sources of hydrazine produced in situ, for example in the production of herbicide precursor 1,2,4-triazole.[7]
Nomenclature
Azines may be named by substitutive or functional class nomenclature.[8][9] In functional class nomenclature, the functional modifier "azine" is appended to the name of the carbonyl compound: hence, "acetone azine". In substitutive nomenclature, azines are named as derivatives of hydrazine: hence, "diisopropylidenehydrazine". In the presence of groups of higher seniority, the prefixes "hydrazinylidene" and "hydrazinediylidene" are used.[10]
References
- ↑ Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995). Pure Appl. Chem. 1995, 67 (8-9), 1307–75 at 1321. DOI: 10.1351/pac199567081307.
- ↑ azines, <http://goldbook.iupac.org/A00557.html> (accessed 2 July 2010), Compendium of Chemical Terminology Internet edition; International Union of Pure and Applied Chemistry (IUPAC).
- ↑ Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995). Pure Appl. Chem. 1995, 67 (8-9), 1307–75 at 1312, 1348. DOI: 10.1351/pac199567081307.
- ↑ aldazines, <http://goldbook.iupac.org/A00207.html> (accessed 2 July 2010), Compendium of Chemical Terminology Internet edition; International Union of Pure and Applied Chemistry (IUPAC). ketazines, <http://goldbook.iupac.org/K03377.html> (accessed 2 July 2010), Compendium of Chemical Terminology Internet edition; International Union of Pure and Applied Chemistry (IUPAC).
- ↑ Day, A. C.; Whiting, M. C. Acetone hydrazone. Org. Synth. 1970, 50, 3, <http://www.orgsyn.org/orgsyn/orgsyn/prepContent.asp?prep=cv6p0010>; Coll. Vol., 6, 10.
- ↑ Gilbert, E. C. Studies on Hydrazine. The Hydrolysis of Dimethylketazine and the Equilibrium between Hydrazine and Acetone. J. Am. Chem. Soc. 1929, 51 (11), 3394–3409. DOI: 10.1021/ja01386a032.
- ↑ Nagata, Nobuhiro; Nishizawa, Chiharu; Kurai, Toshikiyo (Mitsubishi Gas Chemical Co.) Method of producing 1,2,4-triazole. US Patent 6002015, issued 14 December 1999.
- ↑ Rule R-5.6.6.3. In A Guide to IUPAC Nomenclature of Organic Compounds; IUPAC Recommendations 1993; Blackwell Science: Oxford, 1993; p 105. ISBN 0-632-03488-2, <http://www.acdlabs.com/iupac/nomenclature/93/r93_469.htm>.
- ↑ Draft Rule P-68.3.1.2.3. In Nomenclature of Organic Chemistry; IUPAC Provisional Recommendations 2004; IUPAC, 2004, <http://old.iupac.org/reports/provisional/abstract04/favre_310305.html>.
- ↑ Draft Rule P-53.6.2. In Nomenclature of Organic Chemistry; IUPAC Provisional Recommendations 2004; IUPAC, 2004, <http://old.iupac.org/reports/provisional/abstract04/favre_310305.html>.
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