Hofmann-Löffler reaction

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]


The Hofmann-Löffler reaction or Hofmann-Löffler-Freytag Reaction is an organic reaction is which a haloamine is converted to a cyclic amine such as a pyrrolidine with heat and an acid [1][2][3]

An example is the synthesis of n-butylpyrrolidine [4]

Hofmann-Löffler reaction

The reaction type is a radical substitution. In the first step the halogen atom migrates from nitrogen to a gamma or delta carbon position in a rearrangement reaction.

A conceptually related reaction is the Barton reaction.

References

  1. ↑ August Wilhelm von Hofmann (1883). "Ueber die Einwirkung des Broms in alkalischer Lösung auf die Amine (p )". Berichte der deutschen chemischen Gesellschaft. 16 (1): 558–560. doi:10.1002/cber.188301601120.
  2. ↑ Karl Löffler, Curt Freytag (1909). "Über eine neue Bildungsweise von N-alkylierten Pyrrolidinen". Berichte der deutschen chemischen Gesellschaft. 42 (3): 3427–3431. doi:10.1002/cber.19090420377.
  3. ↑ Template:JerryMarch
  4. ↑ Organic Syntheses, Coll. Vol. 3, p.159 (1955); Vol. 25, p.14 (1945). http://www.orgsynth.org/orgsyn/pdfs/CV3P0159.pdf


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