Improving palladium-catalyzed cyanation of aryl halides: development of a state-of-the-art methodology using potassium hexacyanoferrate(II) as cyanating agent |
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Authors: | Thomas Schareina |
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Affiliation: | Leibniz-Institut für Organische Katalyse an der Universität Rostock e.V., Buchbinderstr. 5-6, 18055 Rostock, Germany |
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Abstract: | Benzonitriles are easily accessible via palladium-catalyzed cyanation of aryl halides using potassium hexacyanoferrate(II) as cyanide source. This method is applicable on both activated and deactivated aryl and heteroaryl bromides and activated chlorides giving the corresponding benzonitriles in good to excellent yield. Advantageously, the used cyanating agent is non-toxic and cheap. The presented catalyst system is rather simple and it is not necessary to add expensive phosphines, making the novel method also attractive for industrial applications. |
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Keywords: | Aryl halides Benzonitriles Cyanation Homogeneous catalysis Palladium Potassium hexacyanoferrate(II) |
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