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Auxiliary-directed etherification of sp(2) C–H bonds under heterogeneous metal–organic framework catalysis: synthesis of ethenzamide
An efficient protocol for 8-aminoquinoline assisted alkoxylation and phenoxylation of sp(2) C–H bonds under heterogeneous catalysis was developed. The optimal conditions employed Cu-MOF-74 (20%), K(2)CO(3) base, pyridine ligand or dimethyl formamide solvent, and O(2) oxidant at 80 °C or 100 °C for 2...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077472/ https://www.ncbi.nlm.nih.gov/pubmed/35541499 http://dx.doi.org/10.1039/c7ra12010a |
Sumario: | An efficient protocol for 8-aminoquinoline assisted alkoxylation and phenoxylation of sp(2) C–H bonds under heterogeneous catalysis was developed. The optimal conditions employed Cu-MOF-74 (20%), K(2)CO(3) base, pyridine ligand or dimethyl formamide solvent, and O(2) oxidant at 80 °C or 100 °C for 24 hours. Cu-MOF-74 revealed remarkably higher activity when compared with other previously commonly used Cu-MOFs in cross coupling reactions, supported copper catalysts, and homogeneous copper salts. The reaction scope with respect to coupling partners included a wide range of various substrates. Interestingly, the developed conditions are applicable for the synthesis of high-profile relevant biological agents from easily accessible starting materials. Furthermore, a leaching test confirmed the reaction heterogeneity and the catalyst was reused and recycled at least 8 times with trivial degradation in activity. |
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