A Potential Pathway for the Synthesis of Biomass-Based Polyamide Monomer 2,5-Bis(aminomethyl)furan from 2,5-Furandicarboxylic Acid.

In this study, the transformation of 2,5-furandicarboxylic acid (FDCA) to 2,5-bis(aminomethyl)furan (BAMF) is proposed and investigated for the first time. Using FDCA as the substrate, the process involves two key steps: first, converting FDCA to 2,5-dicyanofuran (DCF) via carboxy-cyanation, followed by the heterogeneous catalytic hydrogenation of DCF to produce BAMF. For the carboxy-cyanation, two ammoniation routes were compared, including the molten ammoniated dehydration route and the moderate ammoniated dehydration route. The difference between the ammoniation of bio-based cyclic dicarboxylic acid and that of petroleum-based aliphatic dicarboxylic acid was discovered. A moderate ammoniated dehydration route that is more suitable for bio-based cyclic dicarboxylic acid has been developed. SOCl2 was found to effectively activate the stable carboxyl group and act as a dehydrating agent, facilitating the dehydration of the intermediate 2,5-furandicarboxamide (FDAM) to DCF with higher efficiency. For the hydrogenation reaction of DCF, Raney Co exhibited excellent catalytic performance, achieving a 94.5% yield of BAMF from DCF. Based on industrial practice, this research represents the first exploration of the pathway from bio-based FDCA to BAMF, which opens a new line for the sustainable production of bio-based diamines.