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Novel Synthetic Reactions Using 1-Fluoro-2, 4, 6-trinitrobenzene. An Efficient Direct Esterification Method

  • Kim Sunggak (Contribution from Department of Chemistry, Korea Advanced Institute of Science and Technology) ;
  • Ahn Kyo Han (Contribution from Department of Chemistry, Korea Advanced Institute of Science and Technology) ;
  • Yang Sungbong (Department of Industrial Chemistry, Ulsan Institute of Technology)
  • 발행 : 1982.06.30

초록

Synthetic utility of 1-fluoro-2,4,6-trinitrobenzene (FTNB) as a condensing agent was investigated. The use of FTNB and DMAP was found to be very effective for direct esterification of carboxylic acids with alcohols or thiols. However, this system was not very effective for macrolactonization. Reaction of 2,4,6-trinitrophenyl esters with several nucleophiles was investigated briefly. Plausible reaction mechanisms of esterification are presented. It seems that the reaction proceeds via the intermediacy of 2,4,6-trinitrophenyl esters by initial formation of 2',4',6'-trinitrophenyl-4-dimethylaminopyridinium salt from which the trinitrophenyl group is transferred to the carboxylic acid.

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참고문헌

  1. Synthetic Commun. S. Kim;S. Yang
  2. Chemistry Lett. S. Kim;S. Yang
  3. J. Org. Chem. v.26 G. S. Shaw;D. L. Seaton .
  4. Bull. Chem. Soc. Japan. v.51 K. Inomata;H. Kinoshita;H. Fukuda;K. Tanabe;H. Kotake
  5. J. Chem. Soc. W. B. Whalley
  6. Angew. Chem. v.81 W. Steglich;G. Hofle
  7. Angew. Chem. Int. Ed. Engl. v.17 G. Hofle;W. Steglich.;H. Vorbruggen
  8. Tetrahedron Lett. v.95 S. K. Chaudhary;O. Hernandez
  9. Tetrahedron Lett. O. Hernandez;S. K. Chaudhary;R. H. Cox;J. Porter
  10. J. Amer. Chem. Soc. v.88 R. B. Woodward;K. Heusler;J. Kosteil;P. Naegeli;W. Oppolzer;R. Ramage;S. Ranganathan;H. Vorbruggen
  11. Tetrahedron Lett. E. J. Corey;M. A. Tius
  12. Angew. Chem. Int. Ed. Engl. v.16 S. Masamune;G. S. Bates.;J. W. Corcoran
  13. Tetrahedron v.33 K. C. Nicolaou
  14. Tetrahedron v.33 T. G. Back
  15. J. Amer. Chem. Soc. v.96 E. J. Coree;K. C. Nicolaou
  16. Bull. Chem. Soc. Japan v.43 E. Endo;S. Ikenaga;T. Mukaiyama
  17. Can. J. Chem. v.53 S. Masamune;S. Kamata;J. Diakur;Y. Sugihara;G. S. Bates
  18. Chemistry Lett. Y. Watanabe. S. Shoda;T. Mukaiyama
  19. J. Org. Chem. v.43 P. A. Grieco;Y. Yoko-hama.;E. Williams
  20. Tetrahedron Lett. T. Cohen;R. E. Gapinski
  21. Angew. Chem. Int. Ed. Engl. v.17 B. Neises;W. Steglich
  22. Tetrahedron Lett. D. N. Harpp;T. Aida.;T. H. Chan
  23. J. Amer. Chem. Soc. v.97 S. Masamune;S. Kamata;W. Schilling
  24. J. Org. Chem. v.42 R. P. Hatch;S. M. Weinreb
  25. Chemistry Lett. H. Kotake;K. Inomata;H. Kinoshita;K. Tanabe;O. Miyano
  26. J. Chem. Soc. A. K. Konasiewicz;A. Maccoll
  27. J. C. S. Chem. Commun. G. Guanti;C. Dell'Erba;F. Pero;G. Leandri
  28. J. C. S. Perkin Il E. Buncel;C. Chuaqui;P. Forsythe;S. Mahoney;A. Raoult;J. F. Wiltshire

피인용 문헌

  1. Bicyclo[3.2.1]octa-3,6-dien-2-yl Cation: A Bishomoantiaromate vol.71, pp.6, 1982, https://doi.org/10.1021/jo0515125