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Study of a Stable "Trifluoromethoxide Anion Solution" Arising from 2,4-Dinitro-Trifluoromethoxybenzene. | LitMetric

Study of a Stable "Trifluoromethoxide Anion Solution" Arising from 2,4-Dinitro-Trifluoromethoxybenzene.

Chemistry

Institute of Chemistry and Biochemistry (ICBMS-UMR CNRS 5246), Univ Lyon, CNRS, Université Lyon 1, 43 Bd du 11 Novembre 1918, 69622, Lyon, France.

Published: November 2021

AI Article Synopsis

  • Trifluoromethoxylation is a tough reaction to carry out, but this research presents a new solution.
  • By combining DMAP with 1,4-dinitro-trifluoromethoxybenzene (DNTFB), a stable trifluoromethoxide anion solution can be created.
  • This stable solution enables S2 reactions without relying on costly silver additives, and the study also explores its properties and behavior.

Article Abstract

Despite recent advances, trifluoromethoxylation remains a challenging reaction. Here we describe an efficient trifluoromethoxylative substitution, using an inexpensive and easy-to-handle reagent. By mixing DMAP with a slight excess of 1,4-dinitro-trifluoromethoxybenzene (DNTFB), a stable solution of trifluoromethoxide anion is obtained and can be used to perform a S 2 reaction without any silver additives. A precise study of the properties and behavior of this unusual stable solution of CF O species is also performed.

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Source
http://dx.doi.org/10.1002/chem.202102809DOI Listing

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