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Acetonitrile–Hexane Extraction Route to Pure Sulfonium Salts

[Image: see text] A rapid, simple procedure is described for synthesizing trialkyl, dialkylaryl, and alkyldiaryl sulfonium salts that features a selective extraction procedure to access analytically pure sulfonium salts. Alkylation of dialkylsulfides, alkylarylsulfides, and diarylsulfides followed b...

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Autores principales: Altundas, Bilal, Kumar, Chepuri V. Suneel, Fleming, Fraser F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288713/
https://www.ncbi.nlm.nih.gov/pubmed/32548524
http://dx.doi.org/10.1021/acsomega.0c01586
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author Altundas, Bilal
Kumar, Chepuri V. Suneel
Fleming, Fraser F.
author_facet Altundas, Bilal
Kumar, Chepuri V. Suneel
Fleming, Fraser F.
author_sort Altundas, Bilal
collection PubMed
description [Image: see text] A rapid, simple procedure is described for synthesizing trialkyl, dialkylaryl, and alkyldiaryl sulfonium salts that features a selective extraction procedure to access analytically pure sulfonium salts. Alkylation of dialkylsulfides, alkylarylsulfides, and diarylsulfides followed by partitioning between acetonitrile and hexanes efficiently separates nonpolar reactants and byproducts, the usual impurities, to afford analytically pure crystalline and noncrystalline sulfonium salts. The method is efficient, general, and particularly well suited for the preparation of oily sulfonium salts that are otherwise extremely difficult to purify.
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spelling pubmed-72887132020-06-15 Acetonitrile–Hexane Extraction Route to Pure Sulfonium Salts Altundas, Bilal Kumar, Chepuri V. Suneel Fleming, Fraser F. ACS Omega [Image: see text] A rapid, simple procedure is described for synthesizing trialkyl, dialkylaryl, and alkyldiaryl sulfonium salts that features a selective extraction procedure to access analytically pure sulfonium salts. Alkylation of dialkylsulfides, alkylarylsulfides, and diarylsulfides followed by partitioning between acetonitrile and hexanes efficiently separates nonpolar reactants and byproducts, the usual impurities, to afford analytically pure crystalline and noncrystalline sulfonium salts. The method is efficient, general, and particularly well suited for the preparation of oily sulfonium salts that are otherwise extremely difficult to purify. American Chemical Society 2020-05-29 /pmc/articles/PMC7288713/ /pubmed/32548524 http://dx.doi.org/10.1021/acsomega.0c01586 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Altundas, Bilal
Kumar, Chepuri V. Suneel
Fleming, Fraser F.
Acetonitrile–Hexane Extraction Route to Pure Sulfonium Salts
title Acetonitrile–Hexane Extraction Route to Pure Sulfonium Salts
title_full Acetonitrile–Hexane Extraction Route to Pure Sulfonium Salts
title_fullStr Acetonitrile–Hexane Extraction Route to Pure Sulfonium Salts
title_full_unstemmed Acetonitrile–Hexane Extraction Route to Pure Sulfonium Salts
title_short Acetonitrile–Hexane Extraction Route to Pure Sulfonium Salts
title_sort acetonitrile–hexane extraction route to pure sulfonium salts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288713/
https://www.ncbi.nlm.nih.gov/pubmed/32548524
http://dx.doi.org/10.1021/acsomega.0c01586
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