生物炼制
化学
氢解
木质素
脱氢
胺化
催化作用
有机化学
还原胺化
生物量(生态学)
胺气处理
木质纤维素生物量
原材料
海洋学
地质学
作者
Bo Zhang,Tenglong Guo,Yuxuan Liu,Fritz E. Kühn,Chao Wang,Zongbao K. Zhao,Jianliang Xiao,Changzhi Li,Tao Zhang
标识
DOI:10.1002/anie.202105973
摘要
Abstract Catalytic conversion of lignin into heteroatom functionalized chemicals is of great importance to bring the biorefinery concept into reality. Herein, a new strategy was designed for direct transformation of lignin β‐O‐4 model compounds into benzylamines and phenols in moderate to excellent yields in the presence of organic amines. The transformation involves dehydrogenation of C α −OH, hydrogenolysis of the C β −O bond and reductive amination in the presence of Pd/C catalyst. Experimental data suggest that the dehydrogenation reaction proceeds over the other two reactions and secondary amines serve as both reducing agents and amine sources in the transformation. Moreover, the concept of “lignin to benzylamines” was demonstrated by a two‐step process. This work represents a first example of synthesis of benzylamines from lignin, thus providing a new opportunity for the sustainable synthesis of benzylamines from renewable biomass, and expanding the products pool of biomass conversion to meet future biorefinery demands.
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