Novel change in rate-determining step within an E1cB mechanism during aminolysis of a sulfamate ester in acetonitrile

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William J. Spillane


Abstract

The observation of biphasic Brønsted plots (β1ca. 0.7 and β2ca. 0) in the aminolysis (alicyclic amines, pyridines) of 4-nitrophenyl N-benzylsulfamate 1a in MeCN is interpreted as being due to a mechanistic change from (ElcB)irrev to (ElcB)rev; the change in rate-determining step occurs at approximately the pKa of 1a and other more basic substrates give straight line plots; an entropy study supports the change from a bimolecular to a unimolecular mechanism.


References

  1. W. J. Spillane, F. A. McHugh and P. O. Burke, J. Chem. Soc., Perkin Trans. 2, 1998, 13 RSC.
  2. W. J. Spillane, G. Hogan, P. McGrath, J. King and C. Brack, J. Chem. Soc., Perkin Trans. 2, 1996, 2099 RSC.
  3. A. F. Cockerill and R. G. Harrison, Mechanisms of elimination and addition reactions involving the X = Y groups, in Chemistry of double-bonded functional groups, ed. S. Patai, Part 1, Supplement A, Wiley, London, 1977 Search PubMed.
  4. A. Williams and K. T. Douglas, J. Chem. Soc., Perkin Trans. 2, 1974, 1727 RSC.
  5. A. Vigroux, M. Bergon, C. Bergonzi and P. Tisnes, J. Am. Chem. Soc., 1994, 116, 11787 CrossRef CAS and earlier papers M. Mowafak Al Sabbagh, M. Calman and J.-P. Calman, J. Chem. Soc., Perkin Trans. 2, 1984, 1233 Search PubMed and earlier papers G. Cevasco and S. Thea, J. Org. Chem., 1995, 60, 70 RSC and earlier papers F. Nome, W. Erbs and V. R. Correia, J. Org. Chem., 1981, 46, 3802 Search PubMed; T. J. Broxton, Aust. J. Chem., 1985, 38, 77 CrossRef CAS; K. T. Leffek and G. Schroeder, Can. J. Chem., 1982, 60, 3077 Search PubMed.
  6. A. Jarczewski and G. Schroeder, Polish J. Chem., 1978, 52, 1985 Search PubMed.
  7. B. R. Cho, S. J. Lee and Y. K. Kim, J. Org. Chem., 1995, 60, 2072 CrossRef CAS The method described was employed to measure the pKas of some of the amines used and was adapted to measure the substrate pKas.
  8. Using the Advanced Chemistry Development (ACD) Inc., Canada, pKa program, which calculates pKa in water, 8.0 was added to the values obtained since this was the approximate difference between calculated (for H2O) and experimental values (in MeCN) for the various series of amines studied.
  9. These are approximate values since the calculations had to be performed without the p-nitro group. The program cannot calculate pKa for compounds with > 20 atoms other than hydrogen.
  10. C. Reichardt, in Solvents and Solvent Effects in Organic Chemistry, 2nd. edn., VCH, Weinheim, 1988, section 4.2 Search PubMed.
  11. J. C. Fishbein and W. P. Jencks, J. Am. Chem. Soc., 1988, 110, 5075 CrossRef CAS and earlier papers.
  12. C. K. M. Heo and J. W. Bunting, J. Org. Chem., 1992, 57, 3570 CrossRef CAS and earlier papers.
  13. S. Thea, N. Kashefi-Naini and A. Williams, J. Chem. Soc., Perkin Trans. 2, 1981, 65 RSC and earlier papers.
  14. J. F. King and R. P. Beatson, Tetrahedron Lett., 1975, 973 CrossRef CAS.
  15. J. L. Kice and L. Weclas, J. Org. Chem., 1985, 50, 32 CrossRef CAS.
  16. M. Caplow, J. Am. Chem. Soc., 1968, 90, 6795 CrossRef CAS.
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