Reaction of Diketoesters of Perfluorodicarboxylic Acids with Alkyl Ketones

Diketoesters were obtained by reacting dialkyl esters of perfluoroadipic and perfluoropimelic acids with alkyl ketones. The features of synthesizing polyfluorinated tetraketones via the reaction of dimethyl perfluorododecanedioate with alkyl ketones were studied. It was found that the use of THF increases the yield of tetraketones. Based on the results of non-empirical MP2/6-31G* calculations of possible stages of the process, details of the reaction mechanism were discussed.

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Publication Details

Journal
Russian Journal of General Chemistry
Published
2026-02-24
DOI
https://doi.org/10.1134/s1070363225603898
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Reaction of Diketoesters of Perfluorodicarboxylic Acids with Alkyl Ketones

Olga Vostrikova, И. А. Новаков, В. В. Бурмистров, Ilya Nazarov et al.
Russian Journal of General Chemistry
Fluorine in Organic Chemistry
article

Reaction of Diketoesters of Perfluorodicarboxylic Acids with Alkyl Ketones

Olga Vostrikova, И. А. Новаков, В. В. Бурмистров, Ilya Nazarov, Sergey V. Chapurkin, Victor V. Chapurkin
article en

Abstract

Diketoesters were obtained by reacting dialkyl esters of perfluoroadipic and perfluoropimelic acids with alkyl ketones. The features of synthesizing polyfluorinated tetraketones via the reaction of dimethyl perfluorododecanedioate with alkyl ketones were studied. It was found that the use of THF increases the yield of tetraketones. Based on the results of non-empirical MP2/6-31G* calculations of possible stages of the process, details of the reaction mechanism were discussed.

Russian Journal of General ChemistryVol. 96(4)
Volgograd State Technical University (RU)
Clean water and sanitation
Openalex Percentile: Top 45%
Fluorine in Organic Chemistry
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