Synthesis 2010(7): 1159-1165  
DOI: 10.1055/s-0029-1219232
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York

A Facile Synthesis of 1-Chloro-2,2,2-trifluoroethyl Sulfides

Yuriy Pustovit*a, Anatoliy Alexeenkoa, Sergii Trofymchuka, Oleg Lukin*b,c, Andrey A. Tolmachevb,c
a Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Murmans’ka St. 5, 02094 Kiev, Ukraine
b National Taras Shevchenko University, ChemBioCenter, Volodymyrska St. 62, 01033 Kiev, Ukraine
c Enamine Ltd., A. Matrosova St. 23, 01103 Kiev, Ukraine
Fax: +380(44)5373253; e-Mail: oleg.lukin@mail.univ.kiev.ua;
Further Information

Publication History

Received 25 September 2009
Publication Date:
20 January 2010 (online)

Abstract

A facile synthesis of structurally diverse 1-chloro-2,2,2-trifluoroethyl sulfides from readily available 1-bromo-1-chloro-2,2,2-trifluoroethane (Halothane®) and various aliphatic and aromatic thiols in the presence of sodium dithionite/sodium bicarbonate is described. The synthetic utility of the prepared sulfides is illustrated by the synthesis of biologically potent heterocycles and by their electrophilic reactions with thiophene.

    References

  • 1a Biomedical Frontiers of Fluorine Chemistry   ACS Symposium Series 639:  Ojima I. McCarthy JR. Welch JT. American Chemical Society; Washington DC: 1996. 
  • 1b Bégué J.-P. Bonnet-Delpon D. Bioorganic and Medicinal Chemistry of Fluorine   Wiley; Hoboken: 2008. 
  • 1c Theodorides G. Fluorine-Containing Agrochemicals, In Advances in Fluorine Science   Vol. 2:  Elsevier; Amsterdam: 2006.  p.121-175  
  • 2 Uneyama K. Momota M. Hayashida K. Itoh T. J. Org. Chem.  1990,  55:  5364 
  • 3 Piettre S. De Cock Ch. Merenyi R. Viehe HG. Tetrahedron  1987,  43:  4309 
  • 4 Fritz H. Sundermeyer W. Chem. Ber.  1989,  122:  1757 
  • 5 Uneyama K. Momota M. Tetrahedron Lett.  1989,  30:  2265 
  • 6 Tournier L. Zard SZ. Tetrahedron Lett.  2005,  46:  455 
  • 7 Kato M. Maeda K. Sato K. Omote M. Ando A. Kumadaki I. Chem. Pharm. Bull.  2000,  48:  683 
  • 8 Wakselman C. Tordeux M. Clavel JL. Langlois B. J. Chem. Soc., Chem. Commun.  1991,  993 
  • 9 Anselmi E. Blazejewski J.-C. Tordeux M. Wakselman C. J. Fluorine Chem.  2000,  105:  41 
  • 10 Huang W.-Y. J. Fluorine Chem.  1992,  58:  1 
  • 11 Gouault S. Pommelet L.-C. Lequeux T. Synlett  2002,  996 
  • 12 Seiichiro H. Satoru N. Akinori K. Tomoko M. Kunitaka M. Toshio F. J. Org. Chem.  1999,  64:  133 
  • 13 Krumkalns EV. inventors; US Patent Application  4282030.  ; Chem. Abstr. 1981, 95, 163901
  • 14 Pustovit Yu. Alekseenko A. Subota A. Tolmachev A. Khim. Geterotsikl. Soedin.  2006,  42:  278