Synthesis 2011(13): 2159-2164  
DOI: 10.1055/s-0030-1260034
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York

A Mild and Efficient Protocol for the Protection of 3-Hydroxychromones Under Phase-Transfer Catalysis

Dmytro Dziuba, Rachid Benhida, Alain Burger*
Laboratoire de Chimie des Molécules Bioactives et des Arômes, UMR 6001 CNRS, Institut de Chimie de Nice, Université de Nice-Sophia Antipolis, 28 avenue de Valrose, 06108 Nice Cedex 2, France
Fax: +33(4)92076151; e-Mail: burger@unice.fr;
Weitere Informationen

Publikationsverlauf

Received 7 March 2011
Publikationsdatum:
06. Mai 2011 (online)

Abstract

A mild and efficient protocol for the introduction of different protecting groups on 3-hydroxychromones (3-HCs) under phase-transfer catalysis conditions in toluene or dichloromethane/aqueous potassium hydroxide system in the presence of crown ether has been developed. The method is useful for the protection of base-sensitive chromone derivatives. Protected chromones are easier to handle and to purify, and therefore suitable for further chemical transformations. The protecting groups were cleaved cleanly using standard conditions.

    References

  • 1a Birt DF. Hendrich S. Wang W. Pharmacol. Ther.  2001,  90:  157 
  • 1b Lee J. Park T. Jeong S. Kim K.-H. Hong C. Bioorg. Med. Chem. Lett.  2007,  17:  1284 
  • 1c Prakash O. Kumar R. Parkash V. Eur. J. Med. Chem.  2008,  43:  435 
  • 2a Klymchenko AS. Demchenko AP. Phys. Chem. Chem. Phys.  2003,  5:  461 
  • 2b Demchenko AP. FEBS Lett.  2006,  580:  2951 
  • 2c Choulier L. Shvadchak VV. Naidoo A. Klymchenko AS. Mély Y. Altschuh D. Anal. Biochem.  2010,  401:  188 
  • 2d Shynkar VV. Klymchenko AS. Kunzelmann C. Duportail G. Muller CD. Demchenko AP. Freyssinet J.-M. Mely Y. J. Am. Chem. Soc.  2007,  129:  2187 
  • 2e Shvadchak VV. Klymchenko AS. de Rocquigny H. Mely Y. Nucleic Acids Res.  2009,  37:  e25/1 
  • 2f Dyrager C. Friberg A. Dahlén K. Chem. Eur. J.  2009,  15:  9417 
  • Typical yields range from 25 to 50%.
  • 3a Yongsheng J, Yuanying J, Qiuye W, Guangquan L, Yang D, and Wenbao L. inventors; Chinese Patent  101244057.  ; Chem. Abstr. 2008, 149, 332105
  • 3b Madhukar M. Sawraj S. Sharma PD. Eur. J. Med. Chem.  2010,  45:  2591 
  • 4 Spadafora M. Postupalenko VY. Shvadchak VV. Klymchenko AS. Mély Y. Burger A. Benhida R. Tetrahedron  2009,  65:  7809 
  • 5 Eckstein F. Oligonucleotides and Analogues   IRL Press; Oxford: 1991.  p.313 
  • PTC conditions were used for the synthesis of alkylated and glycosylated flavonols, see:
  • 6a Demetzos C. Skaltsounis A.-L. Tillequin F. Koch M. Carbohydr. Res.  1990,  207:  131 
  • 6b Gupta SC. Yusuf M. Arora S. Sharma S. Kamboj RC. Dhawan SN. Tetrahedron  2002,  58:  3095 
  • 6c Li Z. Ngojeh G. DeWitt P. Zheng Z. Chen M. Lainhart B. Li V. Felpo P. Tetrahedron Lett.  2008,  49:  7243 
  • 7a McKillop A. Fiaud JC. Hug RP. Tetrahedron  1974,  30:  1379 
  • 7b Reinholz E. Becker A. Synthesis  1990,  1069 
  • 7c Shirakawa S. Yamamoto K. Kitamura M. Ooi T. Maruoka K. Angew. Chem. Int. Ed.  2005,  44:  625 
  • 8 Greene TW. Wuts PGM. Protective Groups in Organic Synthesis   Wiley; New York: 1999.  p.246 
  • 9a Raut KB. Wender SH. J. Org. Chem.  1960,  25:  50 
  • 9b Corvaisier A. Tirouflet J. Compt. Rend.  1960,  251:  1641 
  • 10a Algar J. Flynn JP. Proc. Roy. Irish Acad., Sect. B  1934,  42:  1 ; Chem. Abstr. 1935, 29, 1170
  • 10b Oyamada T. Nippon Kagaku Kaishi  1934,  55:  1256 ; Chem. Abstr. 1935, 29, 33586
  • 10c Baker W. J. Chem. Soc.  1933,  1381 
  • 10d Mahal HS. Venkataraman K. J. Chem. Soc.  1934,  1767 
  • 10e Fougerousse A. Gonzalez E. Brouillard R. J. Org. Chem.  2000,  65:  583 
  • 11 Still WC. Kahn M. Mitra A. J. Org. Chem.  1978,  43:  2923