Selective arene production from transfer hydrogenolysis of benzyl phenyl ether promoted by a co-precipitated Pd/Fe 3 O 4 catalyst
Catalysis Science & Technology, 2016•pubs.rsc.org
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.
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.
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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