Mechanism of the Stevens rearrangement of ammonium ylides

(Note: The full text of this document is currently only available in the PDF Version )

Yasuhiro Maeda and Yoshiro Sato


Abstract

Isomerization of trimethylammonium N-benzylide 2 failed to occur at room temperature in a non-basic medium (HMPA) or at -78 °C in the presence of butyllithium in THF. However, N,N-dimethyl-1-phenylethylamine 4 (Stevens rearrangement product) was formed when the temperature of the latter reaction was raised to room temperature. The mechanism of the Stevens rearrangement is discussed.


References

  1. (a) S. H. Pine, in Organic Reactions, 1970, vol. 18, p. 403 Search PubMed; (b) B. M. Trost and L. S. Melvin Jr., in Sulfur Ylides, Academic Press, New York, 1975 Search PubMed; (c) I. E. Markó, in Comprehensive Organic Synthesis, eds. B. M. Trost and I. Fleming, Pergamon Press, Oxford, 1991, vol. 3, p. 913 Search PubMed; (d) R. Brückner, in Comprehensive Organic Synthesis, eds. B. M. Trost and I. Fleming, Pergamon Press, Oxford, 1991, vol. 6, p. 873 Search PubMed.
  2. (a) J. H. Brewster and M. W. Kline, J. Am. Chem. Soc., 1952, 74, 5179 CrossRef CAS; (b) U. Schöllkopf, U. Ludwig, G. Ostermann and M. Patsch, Tetrahedron Lett., 1969, 39, 3415 CrossRef.
  3. (a) U. Schöllkopf, G. Ostermann and J. Schossigen, Tetrahedron Lett., 1969, 31, 2619 CrossRef; (b) H. Iwamura, M. Iwamura, T. Nishida, M. Yoshida and J. Nakayama, Tetrahedron Lett., 1971, 1, 63 CrossRef; (c) U. H. Dolling, G. L. Closs and A. H. Cohen, J. Chem. Soc., Chem. Commun., 1975, 545 RSC; (d) W. D. Ollis, M. Rey and I. O. Sutherland, J. Chem. Soc., Perkin Trans. 1, 1983, 1009 RSC.
  4. K. P. Klein, D. N. V. Eenam and C. R. Hauser, J. Org. Chem., 1967, 32, 1155 CrossRef CAS.
  5. (a) S. Okazaki, N. Shirai and Y. Sato, J. Org. Chem., 1990, 55, 334 CrossRef CAS; (b) T. Tanaka, N. Shirai, J. Sugimori and Y. Sato, J. Org. Chem., 1992, 57, 5034 CrossRef CAS.
  6. Y. Maeda and Y. Sato, J. Org. Chem., 1996, 61, 5188 CrossRef CAS.
  7. J. March, Advanced Organic Chemistry, 4th edn., John Wiley & Sons, New York, 1992, p. 1101 Search PubMed.
  8. T. Kitano, N. Shirai and Y. Sato, Chem. Pharm. Bull., 1992, 40, 768 CAS.
  9. C. Zhang, Y. Maeda, N. Shirai and Y. Sato, J. Chem. Soc., Perkin Trans. 1, 1997, 25 RSC.
  10. A. Sakuragi, N. Shirai and Y. Sato, J. Org. Chem., 1994, 59, 148 CrossRef CAS.
  11. H. Ahlbrecht, J. Harbach, T. Hauck and H. O. Kalinowski, Chem. Ber., 1992, 125, 1753 CAS.
  12. W. R. Brasen and C. R. Hauser, Org. Synth., Coll. Vol. IV, 1963, 585 Search PubMed.
  13. S. P. James and M. Amin, Can. J. Chem., 1989, 67, 1457.
  14. A. Albert, A. Samuel and P. S. Pregosin, J. Organomet. Chem., 1990, 395, 231 CrossRef.
Click here to see how this site uses Cookies. View our privacy policy here.