Thiete

Thiete
Names
	IUPAC name 2H-thiete
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	2659702 ;
PubChem CID	3415867;
CompTox Dashboard (EPA)	DTXSID30392288 ;
	InChI InChI=1S/C3H4S/c1-2-4-3-1/h1-2H,3H2 Key: HPINPCFOKNNWNW-UHFFFAOYSA-N ; InChI=1/C3H4S/c1-2-4-3-1/h1-2H,3H2 Key: HPINPCFOKNNWNW-UHFFFAOYAF;
	SMILES C1C=CS1;
Properties
Chemical formula	C3H4S
Molar mass	72.12886
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Thiete is a heterocyclic compound containing an unsaturated four-membered ring with three carbon atoms and one sulfur atom.^[1]^[2]^[3] It is more commonly encountered not on its own, but in anellated derivatives, several of which have been synthesized. Thietes are generally not very stable.^[4]

Structure

Thiete is a valence isomer of the unknown compound thioacrolein (CH₂=CHCH=S) Thiete has been shown to be planar, with a C-S-C angle of 76.8 degrees.^[5]

Derivatives

Benzothietes are thietes annulated to benzo group. Such species are prepared by flash vacuum pyrolysis of 2-mercaptobenzyl alcohols. They are precursors to other S-heterocycles.^[6]

Thiete 1,1-dioxides are sulfones, the parent being C₃H₄SO₂. They are more stable than the parent thietes.^[7] Substituted thiete-1,1-dioxides can also be prepared by [2+2] cycloaddition of sulfenes and ynamines.

References

^ Leśniak, S; Lewkowski, J; Kudelska, W; Zając, A (2008). "Thietanes and Thietes: Monocyclic". Comprehensive Heterocyclic Chemistry III. 2.07: 389–428. doi:10.1016/B978-008044992-0.00207-8. {{cite journal}}: Cite has empty unknown parameter: |1= (help)
^ Block, E (2007). "Thietes and Derivatives". Sci. Synth. 33: 187–202. {{cite journal}}: Cite has empty unknown parameter: |1= (help)
^ Block, E; DeWang, M (1996). "Thietanes and Thietes: Monocyclic". Comprehensive Heterocyclic Chemistry II. 1.24: 773–802. doi:10.1016/B978-008096518-5.00024-1. {{cite journal}}: Cite has empty unknown parameter: |1= (help)
^ Dittmer, DC; Davis, FA (1965). "Evidence for a Thiete (Thiacyclobutene)". J. Am. Chem. Soc. 87 (9): 2064–2065. doi:10.1021/ja01087a048.
^ Rodler, M; Bauder, A (1985). "Microwave spectrum, dipole moment and molecular structure of 1,2-dithiete". Chemical Physics Letters. 114: 575–578. doi:10.1016/0009-2614(85)85145-9.
^ Herbert Meier , Axel Mayer, Dieter Gröschl "Benzothietes—versatile Synthons For The Preparation Of Heterocycles" Sulfur Reports, 1994, volume 16, 23-56, doi:10.1080/01961779408048965
^ Thomas C. Sedergran and Donald C. Dittmer "Thiete 1,1-dioxide and Chlorothiete 1,1-dioxide" Org. Synth. 1984, vol. 62, 210.doi:10.15227/orgsyn.062.0210

[1] Leśniak, S; Lewkowski, J; Kudelska, W; Zając, A (2008). "Thietanes and Thietes: Monocyclic". Comprehensive Heterocyclic Chemistry III. 2.07: 389–428. doi:10.1016/B978-008044992-0.00207-8. {{cite journal}}: Cite has empty unknown parameter: |1= (help)

[2] Block, E (2007). "Thietes and Derivatives". Sci. Synth. 33: 187–202. {{cite journal}}: Cite has empty unknown parameter: |1= (help)

[3] Block, E; DeWang, M (1996). "Thietanes and Thietes: Monocyclic". Comprehensive Heterocyclic Chemistry II. 1.24: 773–802. doi:10.1016/B978-008096518-5.00024-1. {{cite journal}}: Cite has empty unknown parameter: |1= (help)

[4] Dittmer, DC; Davis, FA (1965). "Evidence for a Thiete (Thiacyclobutene)". J. Am. Chem. Soc. 87 (9): 2064–2065. doi:10.1021/ja01087a048.

[5] Rodler, M; Bauder, A (1985). "Microwave spectrum, dipole moment and molecular structure of 1,2-dithiete". Chemical Physics Letters. 114: 575–578. doi:10.1016/0009-2614(85)85145-9.

[6] Herbert Meier , Axel Mayer, Dieter Gröschl "Benzothietes—versatile Synthons For The Preparation Of Heterocycles" Sulfur Reports, 1994, volume 16, 23-56, doi:10.1080/01961779408048965

[7] Thomas C. Sedergran and Donald C. Dittmer "Thiete 1,1-dioxide and Chlorothiete 1,1-dioxide" Org. Synth. 1984, vol. 62, 210.doi:10.15227/orgsyn.062.0210

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