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Preparation of 1-cyclopropyl-2-(4′- hydroxy-1′-oxobutyd-cyclopropane

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    Over Raney nickel in the presence of water, the hydrogenation of the furyl ring in 1-cyclopropyl-2-α-furylcyclopropane is accompanied by its hydration without rupture of the cyclopropyl rings.

  2. 2.

    1-Cyclopropyl-2-(4′-hydroxy-1′-oxobutyl)-cyclopropane, 1-cyclopropyl-2-(4′hydroxybutyl)′-cyclopropane, 1,-cyclopropyl-2-(4′-chlorobutyl)-cyclopropane, and 1-cyclopropyl-2-butylcyclopropane have been obtained for the first time.

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Literature cited

  1. A. P. Meshceryakov, V. G. Glukhovtsev, and N. N. Lemin, Izv. AN SSSR, Otd. khim. n., 1901(1961).

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  5. L. Kh. Freidlin, A. P. Meshcheryakov, V. I. Gorshkov, and V. G. Glukhovtsev, Izv. AN SSSR, Otd. khim. n., 2237(1959).

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Authors and Affiliations

  1. The N. D. Zelinskii Institute of Organic Chemistry of the Academy of Sciences of the USSR, USSR

    A. P. Meshcheryakov & V. G. Glukhovtsev

Authors
  1. A. P. Meshcheryakov
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  2. V. G. Glukhovtsev
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Meshcheryakov, A.P., Glukhovtsev, V.G. Preparation of 1-cyclopropyl-2-(4′- hydroxy-1′-oxobutyd-cyclopropane. Russ Chem Bull 10, 2107–2109 (1961). https://doi.org/10.1007/BF01182969

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  • DOI: https://doi.org/10.1007/BF01182969

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