Abstract

AbstractFunneling and functionalization of a mixture of lignin‐derived monomers into a single high‐value chemical is fascinating. Reported herein is a three‐step strategy for the production of terephthalic acid (TPA) from lignin‐derived monomer mixtures, in which redundant, non‐uniform substitutes such as methoxy groups are removed and the desired carboxy groups are introduced. This strategy begins with the hydro‐treatment of corn‐stover‐derived lignin oil over a supported molybdenum catalyst to selectively remove methoxy groups. The generated 4‐alkylphenols are converted into 4‐alkylbenzoic acids by carbonylation with carbon monoxide. The Co‐Mn‐Br catalyst then oxidizes various alkyl chains into carboxy groups, transforming the 4‐alkylbenzoic acid mixture into a single product: TPA. For this route, the overall yields of TPA based on lignin content of corn stover could reach 15.5 wt %, and importantly, TPA with greater than 99 % purity was obtained simply by first decanting the reaction mixture and then washing the solid product with water.

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