Reduction of nitroarenes to azoxybenzenes by potassium borohydride in water

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Abstract

The synthesis of the azoxybenzenes by the reduction of nitroarenes with reducing agent potassium borohydride in water was reported for the first time. PEG-400 was used as a phase transfer catalyst and could effectively catalyze the reduction. The electronic effects of substituent groups play an important role in determining the reduction efficiencies. Electron-withdrawing substituents promote the formation of the azoxybenzene products, while electron-releasing groups retard the reductions to various degrees depending on the extent of their electron-donating ability. © 2011 by the authors.

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Liu, Y., Liu, B., Guo, A., Dong, Z., Jin, S., & Lu, Y. (2011). Reduction of nitroarenes to azoxybenzenes by potassium borohydride in water. Molecules, 16(5), 3563–3568. https://doi.org/10.3390/molecules16053563

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