Exploring Allylation and Claisen Rearrangement as a Novel Chemical Modification of Lignin

Luca Zoia, Anika Salanti, Paola Frigerio, Marco Orlandi


The conversion of lignin into value-added products is traditionally hampered by its stochastic structure and its complex reactivity. The allylation reaction and the aromatic Claisen rearrangement of the allyl group on lignin as chemical modifications are reported for the first time in this work. This approach is aimed at the development of new lignin-based materials and the improvement of its compatibility and ease of processing. In particular, the Claisen rearrangement of lignin is foreseen as a valuable approach to release phenolic groups in an already chemically modified lignin, giving additional reactive sites for further transformation. These reactions were carried out on a purely guaiacylic lignin (TMP), taken as reference material due to its simplicity, and on a more structurally complex herbaceous lignin (P1000®). The Claisen rearrangement of the allylic chain was successfully achieved by treatment in dimethylformamide at reflux temperature for 15 hours. Finally, a screening of the antioxidant activity of reference, allylated, and Claisen rearranged lignins was carried out. Rearranged lignins exhibited satisfactory antioxidant activities if compared to the reference ones.


Allylation; Biorefinery; Claisen rearrangement; 13C NMR; Lignin; 31P NMR

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Welcome to BioResources! This online, peer-reviewed journal is devoted to the science and engineering of biomaterials and chemicals from lignocellulosic sources for new end uses and new capabilities. The editors of BioResources would be very happy to assist you during the process of submitting or reviewing articles. Please note that logging in is required in order to submit or review articles. Martin A. Hubbe, (919) 513-3022, hubbe@ncsu.edu; Lucian A. Lucia, (919) 515-7707, lucian.lucia@gmail.com URLs: bioresourcesjournal.com; http://ncsu.edu/bioresources ISSN: 1930-2126