The catalytic transfer hydrogenolysis of benzyl phenyl ether has been investigated using Pd/Fe3O4 as a heterogeneous catalyst and 2-propanol as a H-donor. After 90 minutes at 240 °C, the cleavage of the ether C–O bond occurs as the only reaction route without hydrogenation of the aromatic ring.

Selective arene production from transfer hydrogenolysis of benzyl phenyl ether promoted by a co-precipitated Pd/Fe3O4 catalyst

E. Paone;R. Pietropaolo;Mauriello F
2016

Abstract

The catalytic transfer hydrogenolysis of benzyl phenyl ether has been investigated using Pd/Fe3O4 as a heterogeneous catalyst and 2-propanol as a H-donor. After 90 minutes at 240 °C, the cleavage of the ether C–O bond occurs as the only reaction route without hydrogenation of the aromatic ring.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.12318/6742
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