Table of Contents
Organic Chemistry International
Volume 2013 (2013), Article ID 502343, 5 pages
http://dx.doi.org/10.1155/2013/502343
Research Article

Rapid and Efficient Synthesis of Hydroxytriarylmethanes under Ultra Sonic Irradiation Using Keggin Heteropolyacids and Preyssler Catalysts in Green Conditions

Department of Chemistry, Payame Noor University (PNU), 19395-4697 Tehran, Iran

Received 25 September 2012; Revised 26 November 2012; Accepted 18 December 2012

Academic Editor: Dipakranjan Mal

Copyright © 2013 Hooshang Hamidian. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. R. Muthyala, A. R. Katritzky, and X. Lan, “A synthetic study on the preparation of triarylmethanes,” Dyes and Pigments, vol. 25, no. 4, pp. 303–324, 1994. View at Google Scholar · View at Scopus
  2. M. Irie, “Light-induced reversible pH change,” Journal of the American Chemical Society, vol. 105, no. 7, pp. 2078–2079, 1983. View at Google Scholar · View at Scopus
  3. P. J. Kocienski, Protecting Groups, Georg Thieme, Stuttgart, Germany, 3rd edition, 2003.
  4. L. Sanguinet, R. J. Twieg, G. Wiggers, G. Mao, K. D. Singer, and R. G. Petschek, “Synthesis and spectral characterization of bisnaphthylmethyl and trinaphthylmethyl cations,” Tetrahedron Letters, vol. 46, no. 31, pp. 5121–5125, 2005. View at Publisher · View at Google Scholar · View at Scopus
  5. S. Kumar Das, Shagufta, and G. Panda, “An easy access to unsymmetric trisubstituted methane derivatives (TRSMs),” Tetrahedron Letters, vol. 46, no. 17, pp. 3097–3102, 2005. View at Publisher · View at Google Scholar · View at Scopus
  6. M. Yamato, K. Hashigaki, Y. Yasumoto et al., “Synthesis and antitumor activity of tropolone derivatives. 6. Structure-activity relationships of antitumor-active tropolone and 8-hydroxyquinoline derivatives,” Journal of Medicinal Chemistry, vol. 30, no. 10, pp. 1897–1900, 1987. View at Google Scholar · View at Scopus
  7. N. Mibu and K. Sumoto, “Preparation of 2,2-dihydroxytriphenylmethanes using metal phenolates with aromatic aldehydes,” Chemical and Pharmaceutical Bulletin, vol. 48, no. 11, pp. 1810–1813, 2000. View at Google Scholar · View at Scopus
  8. M. S. Shchepinov and V. A. Korshun, “Recent applications of bifunctional trityl groups,” Chemical Society Reviews, vol. 32, no. 3, pp. 170–180, 2003. View at Publisher · View at Google Scholar · View at Scopus
  9. C. Grüttner, V. Böhmer, R. Assmus, and S. Scherf, “A convenient and general synthesis of alkanediyl diphenols,” Journal of the Chemical Society, Perkin Transactions 1, no. 2, pp. 93–94, 1995. View at Publisher · View at Google Scholar
  10. M. Gomberg, “On the preparation of triphenylchlomethane,” Journal of the American Chemical Society, vol. 22, pp. 752–757, 1900. View at Publisher · View at Google Scholar
  11. G. Casiraghi, G. Casnati, and M. Cornia, “Regiospecific reactions of phenol salts: reaction-pathways of alkylphenoxy-magnesiumhalides with triethylorthoformate,” Tetrahedron Letters, vol. 14, no. 9, pp. 679–682, 1973. View at Google Scholar · View at Scopus
  12. S. Kumar Das, Shagufta, and G. Panda, “An easy access to unsymmetric trisubstituted methane derivatives (TRSMs),” Tetrahedron Letters, vol. 46, no. 17, pp. 3097–3102, 2005. View at Publisher · View at Google Scholar · View at Scopus
  13. L. M. Werbel, E. F. Elslager, and W. M. Pearlman, “Trisarylmethanes. Synthesis of diarylcarbinol precursors by controlled catalytic hydrogenation,” Journal of Organic Chemistry, vol. 29, no. 4, pp. 967–968, 1964. View at Google Scholar · View at Scopus
  14. M. M. Heravi, S. Sadjadi, S. Sadjadi, H. A. Oskooie, and F. F. Bamoharram, “Rapid and efficient synthesis of 4(3H)-quinazolinones under ultra sonic irradiation using silica-supported Preyssler nano particles,” Ultrasonics Sonochemistry, vol. 16, no. 6, pp. 708–710, 2009. View at Publisher · View at Google Scholar · View at Scopus
  15. M. M. Heravi, F. Derikvand, A. Haeri, H. A. Oskooie, and F. F. Bamoharram, “Heteropolyacids as green and reusable catalysts for the synthesis of isoxazole derivatives,” Synthetic Communications, vol. 38, no. 1, pp. 135–140, 2008. View at Publisher · View at Google Scholar · View at Scopus
  16. T. J. Mason and D. Peters, Practical Sonochemistry, Ellis Horwood, London, UK, 2nd edition, 2002.
  17. “Sonochemistry and Sonoluminiscence,” in Encyclopedia of Physical Science and Technology, K. S. Suslick, Ed., vol. 17, Academic Press, San Diego, Calif, USA, 3rd edition, 2001.
  18. M. M. Heravi, S. Sadjadi, S. Sadjadi, H. A. Oskooie, R. H. Shoar, and F. F. Bamoharram, “Supported preyssler nanoparticles in synthesis of 1,3-diaryl-5- spirohexahydropyrimidines,” Journal of the Chinese Chemical Society, vol. 56, no. 2, pp. 246–250, 2009. View at Google Scholar · View at Scopus
  19. F. Lefebvre, “31P MAS NMR study of H3PW12O40 supported on silica: formation of (SiOH2+)(H2PW12O40),” Journal of the Chemical Society, Chemical Communications, no. 10, pp. 756–757, 1992. View at Publisher · View at Google Scholar · View at Scopus
  20. V. S. Moholkar, P. S. Kumar, and A. B. Pandit, “Hydrodynamic cavitation for sonochemical effects,” Journal of Histochemistry and Cytochemistry, vol. 47, no. 5, pp. 53–65, 1999. View at Google Scholar · View at Scopus