Azirines are heterocyclic organic compounds containing a three-membered ring with two carbon atoms and one nitrogen atom, the unsaturated analogs of aziridines.
| Names | |
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| IUPAC name
2H-Azirine
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| Identifiers | |
3D model (JSmol)
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| 1633516 | |
| ChEBI | |
| ChemSpider | |
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C2H3N | |
| Molar mass | 41.053 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Azirines are heterocyclic organic compounds containing a three-membered ring with two carbon atoms and one nitrogen atom, the unsaturated analogs of aziridines. Azirine, the parent compound, has two isomers: the antiaromatic 1H-azirine, containing a carbon–carbon double bond, is not stable and rearranges to the tautomeric 2H-azirine, containing a carbon–nitrogen double bond, which is at least 30 kcal·mol−1 lower in energy.[1] 2H-Azirines can be considered strained imines and are isolable. They are highly reactive yet have been reported in a few natural products such as dysidazirine.[2]
2H-Azirine is most often obtained by the thermolysis of vinyl azides.[3] During this reaction, a nitrene is formed as an intermediate. Alternatively, they can be obtained by oxidation of the corresponding aziridine. Azirine can be generated during photolysis of isoxazole.[4] Due to the weak N–O bond, the isoxazole ring tends to collapse under UV irradiation, rearranging to azirine.[5]
Substituted azirines can be produced via the Neber rearrangement.
Photolysis of azirines (under 300 nm) is a very efficient way to generate nitrile ylides. These nitrile ylides are dipolar compounds and can be trapped by a variety of dipolarophiles to yield heterocyclic compounds, e.g. pyrrolines.
The strained ring system also undergoes reactions that favor ring opening and can act as a nucleophile or an electrophile.
Azirines readily hydrolyse to give aminoketones which are themselves susceptible to self-condensation.
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