Photolysis of some N-nitroso- and N-nitro-anilines in solution

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

Brian G. Gowenlock, Josef Pfab and Victor M. Young


Abstract

The photolyses of three N-methyl-N-nitrosoanilines and two N-methyl-N-nitroanilines in organic solvents have been studied in the range of 300–340 nm. The influence of solvent character and the presence or absence of oxygen play important roles in the product composition range. The primary photochemical process involves N–N fission, this being homolytic in aprotic solvents and heterolytic in methanol. Three novel mechanistic conclusions are proposed, namely photosolvolysis of a nitrosamine in methanol, photooxidation of nitrosamines in aprotic solvents and the production of biphenyl derivatives on photolysis of nitro-substituted nitrosamines and nitramines in aromatic solvents.


References

  1. B. G. Gowenlock, G. Kresze and J. Pfab, Tetrahedron Lett., 1972, 593 CrossRef CAS; Tetrahedron, 1973, 29, 3587 Search PubMed; Liebigs Ann. Chem., 1975, 1903 Search PubMed; D. Forrest, B. G. Gowenlock and J. Pfab, J. Chem. Soc., Perkin Trans. 2, 1979, 576 Search PubMed.
  2. B. G. Gowenlock, J. Pfab and G. C. Williams, J. Chem. Res. (S), 1978, 362 Search PubMed.
  3. Organic Syntheses, Collective Volume 2, ed. A. H. Blatt, Wiley, New York, 1943, p. 460 Search PubMed.
  4. R. Stoermer, Ber. Dtsch. Chem. Ges., 1898, 31, 2523 Search PubMed.
  5. R. Meldola and E. H. R. Salmon, J. Chem. Soc., 1888, 53, 776 Search PubMed.
  6. Methoden der Organischen Chemie, (Houben-Weyl), ed. E. Müller, Georg Thieme, Stuttgart, 1965, bd. 10/3, p. 557 Search PubMed.
  7. Methoden der Organischen Chemie, (Houben-Weyl), ed. E. Müller, Georg Thieme, Stuttgart, 1958, bd. 11/2, p. 125 Search PubMed.
  8. E. Bamberger, Ber. Dtsch. Chem. Ges., 1894, 27, 359 Search PubMed.
  9. E. D. Hughes and G. T. Jones, J. Chem. Soc., 1950, 2678 RSC.
  10. H. Leymann, Ber. Dtsch. Chem. Ges., 1882, 15, 1235 Search PubMed.
  11. E. Bamberger, Ber. Dtsch. Chem. Ges., 1900, 33, 111.
  12. O. Fischer, Ber. Dtsch. Chem. Ges., 1892, 25, 2841 Search PubMed.
  13. O. Fischer and M. Busch, Ber. Dtsch. Chem. Ges., 1891, 24, 2682 Search PubMed.
  14. J. J. Blanksma, Recl. Trav. Chim. Pays-Bas, 1902, 21, 272.
  15. E. Nötling and Th. Stricker, Ber. Dtsch. Chem. Ges., 1886, 19, 548 Search PubMed.
  16. F. Bell, J. Kenyon and P. H. Robins, J. Chem. Soc., 1926, 1242 RSC.
  17. C. H. Bamford, J. Chem. Soc., 1939, 12 RSC.
  18. G. Geiger and J. R. Huber, Helv. Chim. Acta, 1981, 64, 989 CrossRef CAS.
  19. C. J. Micheida and T. Rydstrom, in N–Nitroso Compounds: Occurrence, Biol. Eff. Relevance Hum. Cancer, vol. 57, IARC Sci. Publ., Lyon, 1984, pp. 365–369 Search PubMed.
  20. E. M. Burgess and J. M. Lavanish, Tetrahedron Lett., 1964, 1221 CrossRef CAS.
  21. N. Fiz, J. L. Usero and J. Casado, Int. J. Chem. Kinet., 1993, 25, 341 CrossRef CAS.