ChemCatChem · 2020 · 69 citations · 51 references
Natural SciencesChemical EngineeringChemistryCatalysisGreen ChemistryOrganic ChemistryCatalyst DesignCatalyst SynthesisCatalytic MaterialsCatalytic MechanismsCatalytic Reaction EngineeringCross-coupling ReactionsCholine Chloride-based SolventsCouplingsDeep Eutectic Solvent CatalysisPalladium CatalystsPalladium-catalyzed Cross-couplingSonogashira Coupling
Abstract The commercially available and cheap Pd/C was found to promote Sonogashira couplings in the environmentally friendly choline chloride/glycerol eutectic mixture in the absence of external ligands. Under heterogeneous conditions, (hetero)aryl iodides were successfully coupled with both aromatic and aliphatic alkynes in yields ranging from 50 to 99 % within 3 h at 60 °C. The aforementioned catalytic system proved to be effective also towards electron‐rich iodides, which are notoriously known to be poorly reactive in Pd‐catalyzed Sonogashira coupling reactions. The eutectic mixture and the catalyst could easily and successfully be recycled up to four times with an E‐factor as low as 24.4.
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Marc Lamblin, Luma Nassar‐Hardy, Jean‐Cyrille Hierso et al. · Advanced Synthesis & Catalysis · 2010 · 639 citations
Matthew R. Netherton, Gregory C. Fu · Organic Letters · 2001 · 598 citations
Solvent effects in palladium catalysed cross-coupling reactions
James Sherwood, James H. Clark, Ian J. S. Fairlamb et al. · Green Chemistry · 2019 · 308 citations · Full text