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Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids

It was demonstrated that the γ-valerolactone-based ionic liquid, tetrabutylphosphonium 4-ethoxyvalerate as a partially bio-based solvent can be utilized as alternative reaction medium for copper- and auxiliary base-free Pd-catalyzed Sonogashira coupling reactions of aryl iodides and functionalized a...

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Autores principales: Orha, László, Tukacs, József M, Kollár, László, Mika, László T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902853/
https://www.ncbi.nlm.nih.gov/pubmed/31839836
http://dx.doi.org/10.3762/bjoc.15.284
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author Orha, László
Tukacs, József M
Kollár, László
Mika, László T
author_facet Orha, László
Tukacs, József M
Kollár, László
Mika, László T
author_sort Orha, László
collection PubMed
description It was demonstrated that the γ-valerolactone-based ionic liquid, tetrabutylphosphonium 4-ethoxyvalerate as a partially bio-based solvent can be utilized as alternative reaction medium for copper- and auxiliary base-free Pd-catalyzed Sonogashira coupling reactions of aryl iodides and functionalized acetylenes under mild conditions. Twenty-two cross-coupling products were isolated with good to excellent yields (72–99%) and purity (>98%). These results represent an example which proves that biomass-derived safer solvents can be utilized efficiently in common, industrially important transformations exhibiting higher chemical and environmental efficiency.
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spelling pubmed-69028532019-12-13 Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids Orha, László Tukacs, József M Kollár, László Mika, László T Beilstein J Org Chem Full Research Paper It was demonstrated that the γ-valerolactone-based ionic liquid, tetrabutylphosphonium 4-ethoxyvalerate as a partially bio-based solvent can be utilized as alternative reaction medium for copper- and auxiliary base-free Pd-catalyzed Sonogashira coupling reactions of aryl iodides and functionalized acetylenes under mild conditions. Twenty-two cross-coupling products were isolated with good to excellent yields (72–99%) and purity (>98%). These results represent an example which proves that biomass-derived safer solvents can be utilized efficiently in common, industrially important transformations exhibiting higher chemical and environmental efficiency. Beilstein-Institut 2019-12-03 /pmc/articles/PMC6902853/ /pubmed/31839836 http://dx.doi.org/10.3762/bjoc.15.284 Text en Copyright © 2019, Orha et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Orha, László
Tukacs, József M
Kollár, László
Mika, László T
Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids
title Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids
title_full Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids
title_fullStr Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids
title_full_unstemmed Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids
title_short Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids
title_sort palladium-catalyzed sonogashira coupling reactions in γ-valerolactone-based ionic liquids
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902853/
https://www.ncbi.nlm.nih.gov/pubmed/31839836
http://dx.doi.org/10.3762/bjoc.15.284
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