DOI QR코드

DOI QR Code

The Effect of Alkali Metal Ions on Reactions of 8-(5-Nitroquinolyl) 3-Furoate with Alkali Metal Ethoxides in Anhydrous Ethanol


Abstract

Pseudo-first-order rate constants have been measured spectrophotometrically for the reactions of 8-(5-nitroquinolyl) 3-furoate with alkali metal ethoxides in anhydrous ethanol. The plot of kobs vs the concentration of alkali metal ethox ides is linear for the reactions performed in the presence of a complexing agent, 18-crown-6 ether, but exhibits upward curvatures for the corresponding reactions performed in the absence of the complexing agent, indicating that the alkali metal ions in this study behave as catalysts. Second-order rate constants were determined for the reactions with dissociated free ethoxide (kEtO-) and with ion paired alkali metal ethoxides (kEtO-M + ) from ion pairing treatments. The magnitude of catalytic effect (kEtO-M + /kEtO-) was found to be 1.7, 3.4 and 2.5 for the reaction of 8-(5-nitroquinolyl) 3-furoate, while 1.4, 3.6 and 4.2 for that of 4-nitrophenyl 2-furoate, 1.8, 3.7 and 2.4 for that of 8-(5-nitroquinolyl) benzoate, and 2.0, 9.8 and 9.3 for that of 8-(5-nitroquinolyl) 2-furoate with EtO- Li+ , EtO- Na+ and EtO- K+ , respectively. A 5-membered chelation at the leaving group is suggested to be responsible for the catalytic effect shown by alkali metal ions.

Keywords

References

  1. Chem. Soc. Rev. v.10 Jencks, W. P.
  2. J. Phys. Org. Chem. v.9 Jencks, W. P.
  3. J. Org. Chem. v.62 Oh, H. K.; Woo, S. Y.; Shin, C. H.; Park, Y. S.; Lee, I.
  4. New J. Chem. v.21 Koh, H. J.; Kim, S. I.; Lee, B. C.; Lee, I.
  5. Bull. Korean Chem. Soc. v.21 Koo, I. S.; Yang, K.; An, S. K.; Lee, C. K.; Lee, I.
  6. Bull. Korean Chem. Soc. v.20 Koo, I. S.; Lee, J. S.; Yang, K.; Kang, K.; Lee, I.
  7. Chem. Commun. Um, I. H.; Kim, M, J.; Lee, H. W.
  8. Bull. Korean Chem. Soc. v.21 Ahn, B. T.; Park, H. S.; Lee, E. J.; Um, I. H.
  9. Chem. Rev. v.99 Castro, E. A.
  10. J. Org. Chem. v.64 Castro, E. A.; Saavedra, C.; Santos, J. G.; Umana, M. J.
  11. J. Org. Chem. v.64 Castro, E. A.; Munoz, P.; Santos, J. G.
  12. J. Am. Chem. Soc. v.122 Baxter, N. J.; Rigoreau, L. J. M.; Laws, A. P.; Page, M. I.
  13. J. Am. Chem. Soc. v.121 Zhang, M.; Brauman, J. I.
  14. J. Am. Chem. Soc. v.120 Adalsteinson, H.; Bruice, T. C.
  15. Acc. Chem. Res. v.22 Williams, A.
  16. Adv. Phys. Org. Chem. v.27 Williams, A.
  17. Chem. Soc. Rev. v.23 Williams, A.
  18. J. Am. Chem. Soc. v.119 Hess, R. A.; Hengge, A. C.; Cleland, W. W.
  19. J. Am. Chem. Soc. v.116 Hengge, A. C.; Hess, R. A.
  20. Acc. Chem. Res. v.26 Fife, T. H.
  21. J. Org. Chem. v.52 Fife, T. H.; Natarajan, R.; Werner, M. H.
  22. Acc. Chem. Res. v.25 Suh, J.
  23. J. Am. Chem. Soc. v.114 Suh, J.; Park, T. H.; Hwang, B. K.
  24. Chem. Soc. Rev. v.24 Pregel, M. J.; Dunn, E. J.; Nagelkerke, R.; Thatcher, G. R. J.; Buncel, E.
  25. Can. J. Chem. v.67 Dunn, E. J.; Buncel, E.
  26. Can. J. Chem. v.68 Pregel, M.; Dunn, E. J.; Buncel, E.
  27. Tetrahedron Lett. v.33 Um, I. H.; Yong, J. I.; Kwon, D. S.; Ahn, B. T.; Lee, I.
  28. Bull. Korean Chem. Soc. v.15 Kown, D. S.; Nahm, J. H.; Um, I. H.
  29. Bull. Korean Chem. Soc. v.19 Um, I. H.; Hong, Y. J.; Lee, Y. J.
  30. Bull. Korean Chem. Soc. Um, I. H.; Lee, S. E.; Min, J. S.
  31. J. Chem. Soc., Perkin Trans. v.2 Mentz, M.; Modro, T. A.
  32. Can. J. Chem. v.72 Mentz, M.; Modro, T. A.; Modro, A. M.
  33. Collect. Czech. Chem. Commun. v.47 Pechanec, V.; Kocian, O.; Zavada, J.
  34. Acc. Chem. Res. v.11 Lehn, J. M.
  35. J. Am. Chem. Soc. v.85 Kurz. J. L.
  36. Acc. Chem. Res. v.5 Wolfenden, R.
  37. Science v.180 Lienhard, G.
  38. Writing Reaction Mechanisms in Organic Chemistry Miller, A.; Solomon, P. H.
  39. Tetrahedron v.53 Um, I. H.; Hong, Y. J.; Kwon, D. S.
  40. J. Org. Chem. v.65 Um, I. H.; Min, J. S.; Ahn, J. A.; Hahn, H. J.
  41. Can. J. Chem. v.77 Um, I. H.; Min, J. S.; Lee, H. W.
  42. J. Chem. Soc., Perkin Trans. v.2 Neuvonen, H.; Neuvonen, K.
  43. In Handbook of Biochemistry. Selected Data for Molecular Biology Jenck, W. P.; Regenstein, J. In(H.A., Ed.)
  44. Contemporary Heterocyclic Chemistry Newkome, J. R.; Paudler, W. W.