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The catalytic synthesis of homologs of pyrrolidine from furan amines

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Summary

1-Furyl-2-alkyl-3-aminopropanes are converted by hydrogenation on platinum in a flowing system at 200–220° to 2-n-propyl-4-alkyl-pyrrofidines with yields of 85–90%.

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Literature cited

  1. 1.

    I. F. Bel'skii and N. I. Shuikin, Dokl. AN SSSR128, 945 (1959).

  2. 2.

    I. F. Bel'skii and N. I. Shuikin, Dokl. AN SSSR137, 331 (1961).

  3. 3.

    N. D. Selinsky and J. K. Jurjew, Ber.64, 101 (1931).

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Bel'skii, I.F. The catalytic synthesis of homologs of pyrrolidine from furan amines. Russ Chem Bull 11, 455–457 (1962). https://doi.org/10.1007/BF00909541

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Keywords

  • Hydrogenation
  • Platinum
  • Furan
  • Flowing System
  • Pyrrolidine