Abstract
The selective reduction of aryl nitro compounds in the presence of sensitive functionalities, including halide, carbonyl, nitrile, and ester substituents, under ultrasonic irradiation at 35 kHz is reported in yields of 39–98%. Iron powder proved superior to stannous chloride with high tolerance of sensitive functional groups and high yields of the desired aryl amines in relatively short reaction times. Simple experimental procedure and purification also make the iron reduction of aryl nitro compounds advantageous over other methods of reduction.
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Acknowledgments
A. B. G. thanks the Australian government for an Australian Postgraduate Award, AVEXA Limited for financial support, and the Centre for Medicinal Chemistry and Pharmacology, UOW, for financial support.