Conclusions
In the reaction of methylmagnesium iodide with esters of perfluorocarboxylic acids, the magnesium salt of the hemiketal was found to be more stable and the ketone yield was found to be higher with increasing bulk of the alkoxy group of the ester.
Literature cited
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1163–1165, May, 1988.
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Batizat, D.V., Yarosh, A.A., Ignatenko, A.V. et al. Reaction of methylmagnesium iodide with perfluorocarboxylate esters. Russ Chem Bull 37, 1022–1024 (1988). https://doi.org/10.1007/BF00957085
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DOI: https://doi.org/10.1007/BF00957085