Conclusions
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1.
Under mild conditions chlorine fluorosulfate chlorinates salts of nitro compounds, replaces the carbethoxy and methylol groups in polynitro derivatives by a chlorine atom, and, depending on the structures of nitro-containing nitriles, either replaces the nitrile group by a chlorine atom or adds on at the C≡N bond.
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2.
Treatment of hydrogen-containing nitromethanes or their salts with peroxydisulfuryl difluoride gave nitromethyl esters of fluorosulfonic acid.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 489–492, March, 1976.
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Fokin, A.V., Studnev, Y.N., Rapkin, A.I. et al. Chlorine fluorosulfate. Russ Chem Bull 25, 472–475 (1976). https://doi.org/10.1007/BF01106634
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DOI: https://doi.org/10.1007/BF01106634