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Fluorosulfonyl-containing heterocyclic compounds

V. Pyrolytic transformations of hexafluoroisobutenylidene sulfate

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

When hexafluoroisobutenylidene sulfate is heated above 80°C, hexafluorodimethylketene is liberated and the inner anhydride of hexafluoro-α-pyrosulfoisobutyric acid (I) is formed. On storage, anhydride I is spontaneously isomerized to hexafluoroisobutenylidene pyrosulfate, which is converted to the mixed anhydride of pentafluoromethacrylic and fluoropyrosulfonic acids on heating above 130° for many hours. On heating above 160°, I is decarboxylated to give hexafluoropropane-2,2-disulfonic acid anhydride, which is inclined to isomerize to pentafluoropropene-2-pyrosulfonyl fluoride.

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Literature cited

  1. G. A. Sokol'skii, V. M. Pavlov, S. A. Agafonov, and I. L. Knunyants, Khim. Geterotsikl. Soed., 178 (1973).

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See [1] for Communication IV.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No, 10, pp. 1321–1324, October, 1973.

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Pavlov, V.M., Derkachev, V.N., Sokol'skii, G.A. et al. Fluorosulfonyl-containing heterocyclic compounds. Chem Heterocycl Compd 9, 1195–1198 (1973). https://doi.org/10.1007/BF00477446

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  • DOI: https://doi.org/10.1007/BF00477446

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