Abstract
The reaction of N-aminoethyleneimine (I) with substituted benzenesulfonyl chlorides (II) has been studied. The main products of the heterolysis of the ring are substituted N′-(Β-chloroethyl)benzenesulfonohydrazides (V). The structure of V has been shown by IR, UV, and PMR spectroscopy, and also by independent synthesis.
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For part III, see [23].
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Hiller, S.A., Eremeev, A.V., Lidak, M.Y. et al. The chemistry of ethyleneimine. Chem Heterocycl Compd 6, 6–8 (1970). https://doi.org/10.1007/BF00475412
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DOI: https://doi.org/10.1007/BF00475412