Synthesis 2016; 48(01): 115-121
DOI: 10.1055/s-0035-1560705
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Aliphatic Azides by Photoinduced C(sp3)–H Azidation

Authors

  • Shin Kamijo*

    a   Graduate School of Science and Engineering, Yamaguchi University, Yamaguchi 753-8512, Japan   Email: kamijo@yamaguchi-u.ac.jp
  • Mizuki Watanabe

    a   Graduate School of Science and Engineering, Yamaguchi University, Yamaguchi 753-8512, Japan   Email: kamijo@yamaguchi-u.ac.jp
  • Kaori Kamijo

    a   Graduate School of Science and Engineering, Yamaguchi University, Yamaguchi 753-8512, Japan   Email: kamijo@yamaguchi-u.ac.jp
  • Keisuke Tao

    a   Graduate School of Science and Engineering, Yamaguchi University, Yamaguchi 753-8512, Japan   Email: kamijo@yamaguchi-u.ac.jp
  • Toshihiro Murafuji

    b   Graduate School of Medicine, Yamaguchi University, Yamaguchi 753-8512, Japan
Further Information

Publication History

Received: 31 August 2015

Accepted after revision: 17 September 2015

Publication Date:
20 October 2015 (online)


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Abstract

A photoinduced synthesis of aliphatic azides was achieved in a single step starting from the parent cyclic alkanes, as well as from tetrahydrofuran and pyrrolidine derivatives. The reaction proceeds via direct azidation of C(sp3)–H bonds in the presence of 4-benzoylpyridine under photoirradiation conditions utilizing tosyl azide as the azide source. The chemoselective C–H mono-azidation at room temperature and the formation of azide compounds in spite of their potential photolability are the key features of the present transformation.

Supporting Information