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Research on furan acetal compounds

X. Hydrogenation of 2-furyl-1.3-dioxanes on raney nickel

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The possibility of the reduction of the furan ring to a tetrahydrofuran ring under the conditions of liquid-phase hydrogenation of 2-furyl-1,3-dioxanes on Raney nickel at atmospheric pressure is demonstrated. 2-Furyl or tetrahydro-2-furyl amino derivatives of 1,3-dioxane are formed in the case of 5-nitro-2-furyl-1,3-dioxanes as a function of the structure of the starting acetals. Data from the UV and IR spectra are presented.

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Authors and Affiliations

  1. Krasnodar Polytechnic Institute, 350006, Krasnodar

    V. G. Kul'nevich, Z. I. Zelikman, Zh. V. Kapustyanskaya, V. G. Glukhovtsev, S. E. Tkachenko & I. S. Zhinzhina

Authors
  1. V. G. Kul'nevich
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  2. Z. I. Zelikman
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  3. Zh. V. Kapustyanskaya
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  4. V. G. Glukhovtsev
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  5. S. E. Tkachenko
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  6. I. S. Zhinzhina
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Additional information

See [1] for communication IX.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1026–1029, August, 1977.

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Kul'nevich, V.G., Zelikman, Z.I., Kapustyanskaya, Z.V. et al. Research on furan acetal compounds. Chem Heterocycl Compd 13, 823–826 (1977). https://doi.org/10.1007/BF00488898

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  • DOI: https://doi.org/10.1007/BF00488898

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