Synthesis of perfluorobiphenyl tetracarboxylic acids <em>via</em> the CuCl<sub>2</sub>-assisted homocoupling of organozinc reagents

New organozinc reagents were obtained from ethyl esters of tetrafluorophenylene dicarboxylic acids in the reaction with Zn and SnCl<sub>2</sub> in DMF. Tetraethyl perfluorobiphenyl tetracarboxylates were synthesized from these organozinc reagents under the action of CuCl<sub>2</sub> and then were hydrolyzed into perfluorobiphenyl tetracarboxylic acids.

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Publication Details

Journal
Mendeleev Communications
Published
2025-01-01
DOI
https://doi.org/10.71267/mencom.7682
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of perfluorobiphenyl tetracarboxylic acids via the CuCl2-assisted homocoupling of organozinc reagents

T. V. Mezhenkova, Vladislav V. Komarov, V. Е. Platonov, A. S. Vinogradov
Mendeleev Communications
Fluorine in Organic Chemistry
article

Synthesis of perfluorobiphenyl tetracarboxylic acids via the CuCl2-assisted homocoupling of organozinc reagents

T. V. Mezhenkova, Vladislav V. Komarov, V. Е. Platonov, A. S. Vinogradov
article en

Abstract

New organozinc reagents were obtained from ethyl esters of tetrafluorophenylene dicarboxylic acids in the reaction with Zn and SnCl<sub>2</sub> in DMF. Tetraethyl perfluorobiphenyl tetracarboxylates were synthesized from these organozinc reagents under the action of CuCl<sub>2</sub> and then were hydrolyzed into perfluorobiphenyl tetracarboxylic acids.

Mendeleev CommunicationsVol. 35(3)
Novosibirsk Institute of Organic Chemistry (RU)
Russian Science Foundation
Openalex Percentile: Top 95%
Fluorine in Organic Chemistry
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