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Synthesis of Primary Amines: First Homogeneously Catalyzed Reductive Amination with Ammonia

机译:伯胺的合成:氨均相催化还原胺化反应

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The synthesis of primary amines via reductive amination of the corresponding carbonyl compounds with aqueous ammonia is achieved for the first time with soluble transition metal complexes. Up to an 86% yield and a 97% selectivity for benzylamines were obtained in the case of various benzaldehydes by using a Rh-catalyst together with water-soluble phosphine and ammonium acetate. In the case of aliphatic aldehydes, a bimetallic catalyst based on Rh/Ir gave improved results.
机译:首次通过可溶性过渡金属络合物实现了通过相应的羰基化合物与氨水的还原胺化反应来合成伯胺。在各种苯甲醛的情况下,通过使用Rh催化剂以及水溶性膦和乙酸铵,可获得高达86%的收率和97%的苄胺选择性。在脂族醛的情况下,基于Rh / Ir的双金属催化剂可改善结果。

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