Oxetene

Chemical compound From Wikipedia, the free encyclopedia

Oxetene is an unsaturated heterocycle. The compound is unstable[citation needed] and has been synthesized.[1] Compared to oxetane, the saturated compound, oxetene is destabilized because the double bond increases the ring strain.[citation needed] Synthesis of some substituted derivatives has been reported.[2][3]

Quick facts Names, Identifiers ...
Oxetene
Names
Preferred IUPAC name
2H-Oxete
Systematic IUPAC name
1-Oxacyclobut-2-ene
Identifiers
3D model (JSmol)
4652799
ChEBI
ChemSpider
  • InChI=1S/C3H4O/c1-2-4-3-1/h1-2H,3H2 checkY
    Key: CRYATLIDHPPXDV-UHFFFAOYSA-N checkY
  • O1\C=C/C1
Properties
C3H4O
Molar mass 56.06326
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
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Oxetene is less studied than oxetane, a related compound that is the base of a number of organic molecules.[2]

Synthesis

Oxetene can be synthesised by the photochemical cyclization of acrolein:[4]

References

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