Abstract
N,N′-dinitrosulfodiamides are formed in the nitration of sulfodiamides with concentrated nitric acid or nitronium borofluoride, and also on substitutional nitration of the corresponding N,N′-di-tert.-butyl derivatives with those reagents. Sulfuryl chloride reacts with the disodium salt of ethylene N,N′-dinitramine to produce 2,5-dinitro-1,2,5-thiadiazolidine-1,1-dioxide. The corresponding N-nitrosulfamides are formed when nitramine salts react with methane sulfochloride.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
Literature cited
A. P. Franchimont, Rec. Trav. Chim. Pays-Bas,3, 417 (1884).
R. Sowada, J. Prakt. Chem.,29, Nos. 3–6, 328 (1965).
Beng Zhongji, Zhang Gengsheng, and Sung Suimin, Binggong Xuebao, No. 1, 9 (1983).
M. Preiss, Chem. Ber.,111, 1915 (1978).
M. Bermann and S. Van Wazer, Synthesis, 576 (1972).
G. Weiss and G. Schulze, Liebigs Ann. Chem.,729, 40 (1969).
O. A. Luk'yanov, T. G. Mel'nikova, L. N. Kriger, and V. A. Tartakovskii, Izv. Akad. Nauk SSSR, Ser. Khim., No. 9, 2138 (1981).
Author information
Authors and Affiliations
Additional information
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1812–1815, August, 1989.
Rights and permissions
About this article
Cite this article
Anikin, O.V., Gareeva, L.G., Chlenov, I.E. et al. N,N′-dialkyl-N,N′-dinitrosulfodiamides. Russ Chem Bull 38, 1659–1663 (1989). https://doi.org/10.1007/BF00956951
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00956951