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Facile synthesis of sulfonyl fluorides from sulfonic acids

Herein, we demonstrate two complementary strategies for the syntheses of sulfonyl fluorides using sulfonic acids and their salts. One strategy involves the conversion of sulfonic acid sodium salts to sulfonyl fluorides using thionyl fluoride in 90–99% yields in one hour. Lessons learned from the mec...

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Autores principales: Thomson, Brodie J., Khasnavis, Samuel R., Grigorian, Emma C., Krishnan, Rohun, Yassa, Theodore D., Lee, Kelvin, Sammis, Glenn M., Ball, Nicholas D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835472/
https://www.ncbi.nlm.nih.gov/pubmed/36503915
http://dx.doi.org/10.1039/d2cc05781f
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author Thomson, Brodie J.
Khasnavis, Samuel R.
Grigorian, Emma C.
Krishnan, Rohun
Yassa, Theodore D.
Lee, Kelvin
Sammis, Glenn M.
Ball, Nicholas D.
author_facet Thomson, Brodie J.
Khasnavis, Samuel R.
Grigorian, Emma C.
Krishnan, Rohun
Yassa, Theodore D.
Lee, Kelvin
Sammis, Glenn M.
Ball, Nicholas D.
author_sort Thomson, Brodie J.
collection PubMed
description Herein, we demonstrate two complementary strategies for the syntheses of sulfonyl fluorides using sulfonic acids and their salts. One strategy involves the conversion of sulfonic acid sodium salts to sulfonyl fluorides using thionyl fluoride in 90–99% yields in one hour. Lessons learned from the mechanism of this reaction also have enabled a complementary deoxyfluorination of sulfonic acids using Xtalfluor-E® – a bench stable solid – allowing for the conversion of both aryl and alkyl sulfonic acids and salts to sulfonyl fluorides in 41–94% yields. Notably, using Xtalfluor-E® enabled milder conditions and the use of both sulfonic acids and their sodium salts.
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spelling pubmed-98354722023-01-14 Facile synthesis of sulfonyl fluorides from sulfonic acids Thomson, Brodie J. Khasnavis, Samuel R. Grigorian, Emma C. Krishnan, Rohun Yassa, Theodore D. Lee, Kelvin Sammis, Glenn M. Ball, Nicholas D. Chem Commun (Camb) Chemistry Herein, we demonstrate two complementary strategies for the syntheses of sulfonyl fluorides using sulfonic acids and their salts. One strategy involves the conversion of sulfonic acid sodium salts to sulfonyl fluorides using thionyl fluoride in 90–99% yields in one hour. Lessons learned from the mechanism of this reaction also have enabled a complementary deoxyfluorination of sulfonic acids using Xtalfluor-E® – a bench stable solid – allowing for the conversion of both aryl and alkyl sulfonic acids and salts to sulfonyl fluorides in 41–94% yields. Notably, using Xtalfluor-E® enabled milder conditions and the use of both sulfonic acids and their sodium salts. The Royal Society of Chemistry 2022-12-06 /pmc/articles/PMC9835472/ /pubmed/36503915 http://dx.doi.org/10.1039/d2cc05781f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Thomson, Brodie J.
Khasnavis, Samuel R.
Grigorian, Emma C.
Krishnan, Rohun
Yassa, Theodore D.
Lee, Kelvin
Sammis, Glenn M.
Ball, Nicholas D.
Facile synthesis of sulfonyl fluorides from sulfonic acids
title Facile synthesis of sulfonyl fluorides from sulfonic acids
title_full Facile synthesis of sulfonyl fluorides from sulfonic acids
title_fullStr Facile synthesis of sulfonyl fluorides from sulfonic acids
title_full_unstemmed Facile synthesis of sulfonyl fluorides from sulfonic acids
title_short Facile synthesis of sulfonyl fluorides from sulfonic acids
title_sort facile synthesis of sulfonyl fluorides from sulfonic acids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835472/
https://www.ncbi.nlm.nih.gov/pubmed/36503915
http://dx.doi.org/10.1039/d2cc05781f
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