Transesterification of Dialkyl Carbonates with 2,2,3,3-Tetrafluoropropan-1-ol


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Abstract

Transesterification of dialkyl carbonates with 2,2,3,3-tetrafluoropropan-1-ol in the presence of various bases leads to the formation of mixtures of bis(2,2,3,3-tetrafluoropropyl) carbonate and alkyl 2,2,3,3-tetrafluoropropyl carbonate. The best catalyst for the synthesis of alkyl 2,2,3,3-tetrafluoropropyl carbonates was found to be tetramethylammonium hydroxide which ensured 81% selectivity for methyl 2,2,3,3-tetrafluoropropyl carbonate, the conversion of dimethyl carbonate being 50%. Lithium alkoxides showed a comparable catalytic efficiency.

About the authors

A. M. Semenova

Postovskii Institute of Organic Synthesis, Ural Branch

Email: pestov@ios.uran.ru
Russian Federation, Yekaterinburg

M. G. Pervova

Postovskii Institute of Organic Synthesis, Ural Branch

Email: pestov@ios.uran.ru
Russian Federation, Yekaterinburg

M. A. Ezhikova

Postovskii Institute of Organic Synthesis, Ural Branch

Email: pestov@ios.uran.ru
Russian Federation, Yekaterinburg

M. I. Kodess

Postovskii Institute of Organic Synthesis, Ural Branch; Yeltsin Ural Federal University

Email: pestov@ios.uran.ru
Russian Federation, Yekaterinburg; Yekaterinburg

A. Ya. Zapevalov

Postovskii Institute of Organic Synthesis, Ural Branch

Email: pestov@ios.uran.ru
Russian Federation, Yekaterinburg

A. V. Pestov

Postovskii Institute of Organic Synthesis, Ural Branch; Yeltsin Ural Federal University

Author for correspondence.
Email: pestov@ios.uran.ru
Russian Federation, Yekaterinburg; Yekaterinburg

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