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Palladium Catalyzed Arylation and Benzylation of Nitroarenes Using Aryl Sulfonates and Benzyl Acetates.

The Journal of organic chemistry (2017-06-16)
Zubaoyi Yi, Yodit Aschenaki, Ryan Daley, Stephen Davick, Abigail Schnaith, Rylee Wander, Dipannita Kalyani
RESUMEN

Pd-catalyzed arylation or benzylation of nitroazoles using aryl sulfonates or benzyl acetates is described. Electronically varied aryl tosylates and mesylates, as well as benzyl acetates, afford the arylated and benzylated products. Arylation of nitrobenzene is also reported. The relative rate for the arylation of halides is greater than that of tosylates using the reported reaction parameters. These studies enhance the scope of electrophiles for nitroarene arylations and benzylations, which was hitherto limited to the use of halide electrophiles.

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Sigma-Aldrich
p-Xylene, anhydrous, ≥99%
Sigma-Aldrich
Cesium pivalate, 98%