Sultine

In chemistry, a sultine is a cyclic ester of a sulfinic acid. This class of organosulfur compounds has few applications. These compounds are typically prepared by the dehydration of hydroxy-sulfinic acids or their equivalent. Illustrative of an alternative route, xylylene dibromide reacts with sodium sulfoxylate (source of SO₂^2-) to give the sultine C₆H₄(CH₂S(O)OCH₂), which is a precursor to o-quinodimethane.^[1]

References

^ Dittmer, Donald C.; Hoey, Michael D. (1981). "Cyclic Sulphinic Acid Derivatives (Sultines and Sulphinamides)". In Saul Patai (ed.). Sulphinic Acids, Esters and Derivatives. PATAI'S Chemistry of Functional Groups. John Wiley & Sons. p. 239-273. doi:10.1002/9780470772270.ch9. ISBN 9780470772270.

[Patai-1] Dittmer, Donald C.; Hoey, Michael D. (1981). "Cyclic Sulphinic Acid Derivatives (Sultines and Sulphinamides)". In Saul Patai (ed.). Sulphinic Acids, Esters and Derivatives. PATAI'S Chemistry of Functional Groups. John Wiley & Sons. p. 239-273. doi:10.1002/9780470772270.ch9. ISBN 9780470772270.

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