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Ionic Liquid-Promoted Three-Component Domino Reaction of Propargyl Alcohols, Carbon Dioxide and 2-Aminoethanols: A Thermodynamically Favorable Synthesis of 2-Oxazolidinones
To circumvent the thermodynamic limitation of the synthesis of oxazolidinones starting from 2-aminoethanols and CO(2) and realize incorporation CO(2) under atmospheric pressure, a protic ionic liquid-facilitated three-component reaction of propargyl alcohols, CO(2) and 2-aminoethanols was developed...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280151/ https://www.ncbi.nlm.nih.gov/pubmed/30463369 http://dx.doi.org/10.3390/molecules23113033 |
Sumario: | To circumvent the thermodynamic limitation of the synthesis of oxazolidinones starting from 2-aminoethanols and CO(2) and realize incorporation CO(2) under atmospheric pressure, a protic ionic liquid-facilitated three-component reaction of propargyl alcohols, CO(2) and 2-aminoethanols was developed to produce 2-oxazolidinones along with equal amount of α-hydroxyl ketones. The ionic liquid structure, reaction temperature and reaction time were in detail investigated. And 15 mol% 1,5,7-triazabicylo[4.4.0]dec-5-ene ([TBDH][TFE]) trifluoroethanol was found to be able to synergistically activate the substrate and CO(2), thus catalyzing this cascade reaction under atmospheric CO(2) pressure. By employing this task-specific ionic liquid as sustainable catalyst, 2-aminoethanols with different substituents were successfully transformed to 2-oxazolidinones with moderate to excellent yield after 12 h at 80 °C. |
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