Oxidation of lignin and lignin β-O-4 model compounds via activated dimethyl sulfoxide

Lignin oxidation reactions are increasingly being utilized in the field of lignin valorization. This is primarily due to the prospect of obtaining high-value aromatic products from cleavage of the C-alpha-C-beta bond in lignin's beta-O-4 linkages. In this work activated dimethyl sulfoxide reactions, namely Swern and Parikh-Doering oxidations, were performed both on lignin and on compounds modeling the beta-O-4 linkage. When phenolic moieties were present in the model compounds, enol ethers were formed rather than the ketone expected from oxidation of the beta-O-4 alcohol moiety. Conversely, in the absence of phenolic moieties, the beta-O-4 alcohol was oxidized to a ketone. These results are interpreted in terms of enol ether formation from a quinone methide intermediate formed via deprotonation of the phenolic -OH in the initial sulfur ylide species. When applied to Kraft lignin, alcohol oxidation was observed at both the alpha and gamma positions in lignin under both Swern and Parikh-Doering conditions, although analytical data were unable to shed light on the relative importance of enol ether versus 1,3-diketone formation (or its tautomer). These results emphasize the importance of working with realistic lignin model compounds in order to understand and develop lignin chemistry.