Abstract
The reaction of aziridine with trialkylsilanethiols in dry tetrahydrofuran (THF) at 55–60°C, which leads to the formation of mixtures of substances [according to the data from the IR and PMR spectra, hexalkyldisilyl sulfides, 2-mercaptoethylamine, trialkyl(2-aminoethylthio)silanes, and 1-trialkylsilylamino-2-trialkylsilylthioethanes], was studied. 2-Mercaptoethylamine and 1-trialkylsilylamino-2-trialkyl-silylthioethanes, the structures of which were established on the basis of the IR and PMR spectra, were isolated in pure form.
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See [1] for communication 10.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1652–1653, December, 1979.
Original submitted August 11, 1978.
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Voronkov, M.G., Knutov, V.I., Chudesova, L.M. et al. Heteroatomic derivatives of aziridine. Chem Heterocycl Compd 15, 1327–1329 (1979). https://doi.org/10.1007/BF00514736
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DOI: https://doi.org/10.1007/BF00514736