Recyclable and reusable NiCl2(PPh3)2/CuI/PEG-400/H2O system for the sonogashira coupling reaction of aryl iodides with alkynes

A stable and highly efficient NiCl2(PPh3)2/CuI/PEG‐400/H2O catalytic system for the Sonogashira reaction has been developed. In the presence of NiCl2(PPh3)2 and CuI, the coupling reaction of aryl iodides with terminal alkynes was carried out smoothly in a mixture of poly(ethylene glycol) (PEG‐400) a...

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Veröffentlicht in:Applied organometallic chemistry 2015-12, Vol.29 (12), p.846-849
Hauptverfasser: Wei, Ting, Zhang, Tingli, Huang, Bin, Tuo, Yuxin, Cai, Mingzhong
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Sprache:eng
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Zusammenfassung:A stable and highly efficient NiCl2(PPh3)2/CuI/PEG‐400/H2O catalytic system for the Sonogashira reaction has been developed. In the presence of NiCl2(PPh3)2 and CuI, the coupling reaction of aryl iodides with terminal alkynes was carried out smoothly in a mixture of poly(ethylene glycol) (PEG‐400) and water at 100°C with K2CO3 as base to afford a variety of arylacetylenes in good to excellent yields. The isolation of the products was readily performed by extraction with petroleum ether, and the NiCl2(PPh3)2/CuI/PEG‐400/H2O system could be easily recycled and reused six times without significant loss of catalytic activity. Our system not only avoids the use of easily volatile organic solvents but also solves the basic problem of catalyst reuse. Copyright © 2015 John Wiley & Sons, Ltd. A highly efficient and reusable NiCl2(PPh3)2/CuI/PEG‐400/H2O system for the Sonogashira coupling reaction of aryl iodides with terminal alkynes has been developed. The reactions generated a variety of arylacetylenes in good to excellent yields, and the NiCl2(PPh3)2/CuI/PEG‐400/H2O system could be easily recycled and reused six times without significant loss of catalytic activity.
ISSN:0268-2605
1099-0739
DOI:10.1002/aoc.3394