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A series of N-monoalkyl aromatic amines are synthesized in high yields from corresponding nitroarene derivatives,aldehydes,and ammonium formate in the presence of Pd/C as a catalyst through one-pot operations at room temperature. Both the conversion and selectivity of the process are above 80%. Optimum reaction conditions are investigated,and it is found that the optimum molar ratio of nitroarene derivatives to ammonium formate and the optimum weight ratio of nitroarene derivatives to Pd/C are 1/4 and 1/0.10,respectively. These experiments provide a novel access for N-monoalkyl aromatic amines with advantages of simplicity,high selectivity,and environmental benignity.
A series of N-monoalkyl aromatic amines are synthesized in high yields from corresponding nitroarene derivatives, aldehydes, and ammonium formate in the presence of Pd / C as a catalyst through one-pot operations at room temperature. Both the conversion and selectivity of the process are above 80%. Optimum reaction conditions are investigated, and it is found that the optimum molar ratio of nitroarene derivatives to ammonium formate and the optimum weight ratio of nitroarene derivatives to Pd / C are 1/4 and 1 / 0.10, respectively. These are experiments provide a novel access for N-monoalkyl aromatic amines with advantages of simplicity, high selectivity, and environmental benignity.