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Substituent-controlled, mild oxidative fluorination of iodoarenes: synthesis and structural study of aryl I(iii)- and I(v)-fluorides
We report a mild approach to the synthesis of difluoro(aryl)-λ(3)-iodanes (aryl-IF(2) compounds) and tetrafluoro(aryl)-λ(5)-iodanes (aryl-IF(4) compounds) using trichloroisocyanuric acid (TCICA) and potassium fluoride (KF). Under these reaction conditions, selective access to either the I(iii)- or I...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685355/ https://www.ncbi.nlm.nih.gov/pubmed/31588294 http://dx.doi.org/10.1039/c9sc02162k |
Sumario: | We report a mild approach to the synthesis of difluoro(aryl)-λ(3)-iodanes (aryl-IF(2) compounds) and tetrafluoro(aryl)-λ(5)-iodanes (aryl-IF(4) compounds) using trichloroisocyanuric acid (TCICA) and potassium fluoride (KF). Under these reaction conditions, selective access to either the I(iii)- or I(v)-derivatives is predictable based solely on the substitution pattern of the iodoarene starting material. Moreover, the discovery of this TCICA/KF approach prompted detailed dynamic NMR, kinetic, computational, and crystallographic studies on the relationship between the IF(2) group and the ortho-substituents on carefully designed probe molecules. It was during these experiments that the role of the ortho-substituent in inhibiting further oxidative fluorination of I(iii)-compounds to I(v)-compounds during the reaction with TCICA and KF was revealed. Additionally, a notable exception to this empirical trend is discussed herein. |
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