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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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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. |
format | Online Article Text |
id | pubmed-9835472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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