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Structure of adducts of bis(trifluoromethyl)ketene with methoxymethylamines and diaminomethanes

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 1.

    By means of the IR, NMR, and mass spectra of the reaction products of alkoxymethylamines and diaminomethanes with bis(trifluoromethyl)ketene it was shown that these adducts are formed via addition to the C=C bond of the starting ketene.

  2. 2.

    The counter synthesis of the esters ofα-morpholinomethylhexafluoroisobutyric acid was accomplished by the Mannich condensation of the esters ofα-hydrohexafluoroisobutyric acid with methoxy-methylm rpholine.

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 176–179, January, 1973.

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Urushadze, M.V., Abduganiev, E.G., Samoilova, Z.E. et al. Structure of adducts of bis(trifluoromethyl)ketene with methoxymethylamines and diaminomethanes. Russ Chem Bull 22, 182–184 (1973). https://doi.org/10.1007/BF00854158

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  • DOI: https://doi.org/10.1007/BF00854158

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