Abstract
AbstractMixed alkyl/aryl diphos ligands have been prepared and their application in iron‐catalyzed cross coupling of benzylic chlorides with diaryl zinc (Negishi) or aryl Grignard reagents (Kumada) towards the synthesis of diarylmethane has been evaluated. The iron−diphos catalytic system exhibited the enhanced activity and selectivity in the two coupling reactions. The electron‐rich mixed PPh2/PCy2 ligands outperformed their symmetrical PPh2 congeners, and led to decreased homocoupling byproduct formation. It indicates that the electronic effect of the ligands plays an important role in the catalytic performance. The Fe catalyst supported by L8 bearing an electron‐rich PCy2 substituent and a sterically demanding tert‐butyl on ethene backbone exhibited the best catalytic performance and good functional group tolerance in the two cross coupling reactions.
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