Synthesis 2014; 46(11): 1448-1454
DOI: 10.1055/s-0033-1341249
practical synthetic procedures
© Georg Thieme Verlag Stuttgart · New York

Preparation of Aromatic Triazenes and Their Application in Silver-Mediated Perfluoroalkylation Reactions

Authors

  • Andreas Hafner

    a   Institute of Organic Chemistry, KIT-Campus South, Fritz-Haber-Weg 6, 76131 Karlsruhe, Germany   Fax: +49(721)60848581   Email: braese@kit.edu
  • Christoph Hussal

    a   Institute of Organic Chemistry, KIT-Campus South, Fritz-Haber-Weg 6, 76131 Karlsruhe, Germany   Fax: +49(721)60848581   Email: braese@kit.edu
  • Stefan Bräse*

    a   Institute of Organic Chemistry, KIT-Campus South, Fritz-Haber-Weg 6, 76131 Karlsruhe, Germany   Fax: +49(721)60848581   Email: braese@kit.edu
    b   Institute of Toxicology and Genetics, KIT, Campus-North, Hermann-von-Helmholtz Platz 1, 76344 Eggenstein-Leopoldshafen, Germany
Further Information

Publication History

Received: 02 April 2014

Accepted after revision: 04 April 2014

Publication Date:
30 April 2014 (online)


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Abstract

Herein, the syntheses of various functionalized 1,3-diisopropyltriaz-1-enes is described. This simple transformation tolerates a vast number of functional groups (e.g., halides) and allows the syntheses of 1,3-diisopropyltriaz-1-enes starting from commercially available aniline derivatives. These substrates are suitable for a range of silver-mediated perfluoroalkylation reactions.