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. 2023 Dec 1;13(48):34273–34290. doi: 10.1039/d3ra06533b

Comparison of the activity of this method with reported methods for the preparation of benzophenone (product 4a).

Entry Catalytic system Conditions Yield (%) [ref]
1 PdCl2/([(PhNH)P2(NPh)2]2NPh) KOAc/PEG, 90 °C, 10 h 78% (ref. 52)
2 [(Cinnamyl)PdCl]2/DPEphos DCC, THF, 120 °C, 24 h 63% (ref. 46)
3 Fe3O4@SiO2–2P–PdCl2 DCC, toluene, K2CO3, 100 °C, 12 h 85% (ref. 47)
4 Pd-APDMS Anisole, K2CO3, 100 °C, 5 h 60% (ref. 45)
5 Pd(OAc)2, DMAP KOH, toluene, 80 °C, 12 h 75% (ref. 41)
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