Conclusions
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1.
The electrophillic cleavage of alkyl fluorides from the esters ofα-trifluoromethyl-β,β-dialkoxy-acrylic acids leads to the formation of esters of difluoromethylenemalonic acid.
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2.
During the reaction between the dimethyl ester of difluoromethylenemalonic acid and trimethylphosphite, a stable adduct is formed, which when heated splits into methyl difluorophosphite and the dimethyl ester of dimethoxymethylenemalonic acid.
Literature cited
I. L. Knunyants, Yu. G. Abduganiev, E. M. Rokhlin, P. O. Okulevich, and N. I. Karpushina, Tetrahedron,29, 595 (1973).
U. Utabaev, E. M. Rokhlin, É. P. Lur'e, and I. L. Knunyants, Izv. Akad. Nauk SSSR, Ser. Khim., 1463 (1975).
L. A. Rozov, Yu. V. Zeifman, Yu. A. Cheburkov, and I. L. Knunyants, Izv. Akad. Nauk SSSR, Ser. Khim., 372 (1976).
L. L. Knunyants, Yu. A. Cheburkov, M. D. Bargamova, É. I. Fedin, and P. V. Petrovskii, Izv, Akad. Nauk SSSR, Ser. Khim., 1031 (1966).
I. L. Knunyants, V. V. Tyulenéva, E. Ya. Pervova, and R. N. Sterlin, Izv. Akad. Nauk SSSR, Ser. Khim., 1797 (1964).
I. L. Kunyants, S. T. Kocharyan, Yu. A. Cheburkov, M. D. Bargamova, and E. M. Rokhlin, Dokl. Akad. Nauk SSSR,165, 827 (1965).
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 895–897, April, 1976.
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Knunyants, I.L., Utebaev, U., Rokhlin, E.M. et al. Synthesis of difluoromethylenemalonic acid esters and their reactions with trialkyl phosphites. Russ Chem Bull 25, 873–875 (1976). https://doi.org/10.1007/BF00922400
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DOI: https://doi.org/10.1007/BF00922400