A method for preparing amine compounds using a reversed-phase metal catalyst
By using non-precious metal reversed-phase catalysts such as reversed-phase CeOx/Ni and reversed-phase CeYOx/Co, a highly efficient hydrogenation amination reaction using lignin-based phenolic compounds as raw materials was achieved, solving the problem of high cost of precious metal catalysts and realizing the green synthesis of high-value-added amine compounds.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- NANJING TECH UNIV
- Filing Date
- 2026-04-20
- Publication Date
- 2026-07-10
AI Technical Summary
In existing technologies, precious metal catalysts are expensive and dependent on non-renewable resources, which limits the large-scale application and raw material adaptability of lignin-derived aromatic monomers, making it difficult to efficiently prepare high-value-added amine compounds such as 4,4'-methylenediphenylamine and hexamethylenediamine.
Using non-precious metal reversed-phase catalysts, such as reversed-phase CeOx/Ni and reversed-phase CeYOx/Co, lignin-based phenolic compounds are converted into amine compounds through hydrogenation amination reactions. The reaction is carried out in two or one steps under hydrogen and ammonia atmospheres using reversed-phase nickel/cobalt-based metal catalysts.
It enables the efficient preparation of a series of monocyclic anilines and complex bicyclic amines in a green and sustainable manner, with selectivity and yield reaching 80%-90%. It is applicable to structurally complex compounds, reduces costs, and improves the adaptability of raw materials.
Smart Images

Figure CN122355835A_ABST