Synthesis 2004(7): 1003-1006  
DOI: 10.1055/s-2004-822338
PAPER
© Georg Thieme Verlag Stuttgart · New York

Dod-S-Me and Methyl 6-Morpholinohexyl Sulfide (MMS) as New Odorless Borane Carriers

Pranab K. Patra, Kiyoharu Nishide*, Kaoru Fuji, Manabu Node*
Department of Pharmaceutical Manufacturing Chemistry, Kyoto Pharmaceutical University, Misasagi, Yamashina, Kyoto 607-8414, Japan
Fax: +81(75)5954775; e-Mail: nishide@mb.kyoto-phu.ac.jp; e-Mail: node@mb.kyoto-phu.ac.jp;
Further Information

Publication History

Received 26 January 2004
Publication Date:
14 April 2004 (online)

Abstract

Odorless Dod-S-Me (1) and MMS (3) are developed as efficient borane carriers. The yields of hydroborations and reductions with borane complex 2 of 1 are very high and the recovery of 1 after the reaction is quantitative. The borane complexes 4 and 5 of 3 are also useful. In the latter case chromatographic separation is unnecessary when excess oxidizing agent (alkaline H2O2) is used after hydroboration.

    References

  • 1a Solladie G. Synthesis of Sulfides, Sulfoxides and Sulfones, In Comprehensive Organic Synthesis   Vol. 6:  Trost BM. Fleming I. Pergamon Press; Oxford UK: 1991.  p.133-170 
  • 1b Procter DJ. J. Chem. Soc., Perkin Trans. 1  2001,  335 
  • 1c Roy K.-M. Thiols and Organic Sulfides, In Ullmann’s Encyclopedia of Industrial Chemistry   Wiley-VCH; Weinheim: 2002. 
  • 2a Harris JM. Liu Y. Chai S. Andrews MD. Vederas JC. J. Org. Chem.  1998,  63:  2407 
  • 2b Cole CD. Stock JR. Kappel JA. Bioorg. Med. Chem. Lett.  2002,  12:  1791 
  • 2c Crich D. Neelamkavil S. J. Am. Chem. Soc.  2001,  123:  7449 
  • 2d Crich D. Neelamkavil S. Tetrahedron  2002,  58:  3865 
  • 3a Nishide K. Ohsugi S. Fudesaka M. Kodama S. Node M. Tetrahedron Lett.  2002,  43:  5177 
  • 3b Ohsugi S. Nishide K. Oono K. Okuyama K. Fudesaka M. Kodama S. Node M. Tetrahedron  2003,  59:  8393 
  • 3c For the references related to odorless thiols, see the following: Nishide K. Ohsugi S. Shiraki H. Tamakita H. Node M. Org Lett.  2001,  3:  3121 
  • 3d Node M. Kumar K. Nishide K. Ohsugi S. Miyamoto T. Tetrahedron Lett.  2001,  42:  9207 
  • 3e Nishide K. Miyamoto T. Kumar K. Ohsugi S. Node M. Tetrahedron Lett.  2002,  43:  8569 
  • 4a Zaidlewicz M. Brown HC. Encyclopedia of Reagents for Organic Synthesis   Vol. 1:  J. Wiley; New york: 1995.  p.634 
  • 4b Brown HC. Organic Syntheses via Boranes   Aldrich Chemical Co. Inc.; Milwaukee: 1997. 
  • 5a 1,2-Bis(tert-butylthio)ethane and 1,4-bis(benzyl-thio)butane: Follet M. Chem. Ind.  1986,  123 
  • 5b 1,4-Thio-xane: Brown HC. Mandal AK. J. Org. Chem.  1992,  57:  4970 
  • 5c Diisoamyl sulfide and bis(2-methoxyethyl)sulfide: Zaidlewicz M. Kanth JVB. Brown HC. J. Org. Chem.  2000,  65:  6697 
  • 5d Bis(2-hydroxyethyl)sulfide: Brown HC. Zaidlewicz M. Dalvi PK. Biswas GK. J. Org. Chem.  2001,  66:  4795 
  • 5e 2-(Perfluorooctyl)ethyl methyl sulfide: Crich D. Neelamkavil S. Org Lett.  2002,  4:  4175 
  • 6 Nishide K. Patra PK. Matoba M. Shanmugasundaram K. Node M. Green Chem.  2004,  4:  142 
  • 7 Zwifel G. Brown HC. Org. React.  1963,  13:  1 
  • 8 Brown HC. Kanth JVB. Dalvi PK. Zaidlewicz M. J. Org. Chem.  1999,  64:  6263