Abstract
1-Alkyl-substituted 1,5-diketones react with sulfurous reagents (H2S and P4S10) to give thiopyrylium salts primarily via a mechanism that is competitive with disproportionation. The reaction depends on the nature of the acidic reagent. Some properties of the compounds obtained are described.
Similar content being viewed by others
Literature cited
V. G. Kharchenko, M. E. Stankevich, and N. M. Kupranets, Zh. Org. Khim., 8, 193 (1972).
F. Duus, J. Org. Chem., 42, 3123 (1972).
V. G. Kharchenko, N. I. Kozhevnikova, and N. V. Voronina, Khim. Geterotsikl. Soedin., No. 4, 562 (1979).
I. Strating and E. Molenaar, Org. Prep. Proced., 1, 21 (1969).
H. Hartman, J. Prakt. Chem., 313, 1113 (1971).
M. N. Tilichenko and V. G. Kharchenko, Zh. Obshch. Khim., 29, 1911 (1959).
E. F. Dstensen, A. A. A. Abdalach, S. H. Skaaze, and M. M. Mishrikey, Acta Chem. Scand., 832, 496 (1977).
Koichi Narasaka, Kenso Soui, and Teruaku Mukaiyama, Chem. Lett., No. 10, 1223 (1974).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 762–766, June, 1981.
Rights and permissions
About this article
Cite this article
Kharchenko, V.G., Chalaya, S.N. & Chichenkova, L.G. Synthesis and reactions of 1-Alkyl-substituted 1,5-diketones with sulfurous reagents. Chem Heterocycl Compd 17, 557–560 (1981). https://doi.org/10.1007/BF00503479
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00503479