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Synthesis, structure, and transformations of cyclic glycerol formals

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Abstract

Glycerol reacts with paraformaldehyde to give a mixture of 4-hydroxymethyl-1,3-dioxolane and 5-hydroxy-1,3-dioxane. Some transformations (alkylation and replacement of the OH groups with the Cl atoms) of the synthesized compounds were performed. The differences in NMR and mass spectra of the corresponding 1,3-dioxolanes and 1,3-dioxanes were revealed and discussed.

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Authors and Affiliations

  1. Ufa State Petroleum Technological University, 1 ul. Kosmonavtov, 450062, Ufa, Russian Federation

    G. Z. Raskildina, V. F. Valiev, R. M. Sultanova & S. S. Zlotsky

Authors
  1. G. Z. Raskildina
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  2. V. F. Valiev
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  3. R. M. Sultanova
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  4. S. S. Zlotsky
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Corresponding author

Correspondence to G. Z. Raskildina.

Additional information

Dedicated to Academician of the Russian Academy of Sciences N. S. Zefirov on the occasion of his 80th birthday.

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 2095–2099, September, 2015.

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Raskildina, G.Z., Valiev, V.F., Sultanova, R.M. et al. Synthesis, structure, and transformations of cyclic glycerol formals. Russ Chem Bull 64, 2095–2099 (2015). https://doi.org/10.1007/s11172-015-1123-z

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  • DOI: https://doi.org/10.1007/s11172-015-1123-z

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