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Solvent‐Promoted Oxidation of Aromatic Alcohols/Aldehydes to Carboxylic Acids by a Laccase‐TEMPO System: Efficient Access to 2,5‐Furandicarboxylic Acid and 5‐Methyl‐2‐Pyrazinecarboxylic Acid
Author(s) -
Cheng AiDi,
Zong MinHua,
Lu GuangHui,
Li Ning
Publication year - 2021
Publication title -
advanced sustainable systems
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.499
H-Index - 24
ISSN - 2366-7486
DOI - 10.1002/adsu.202000297
Subject(s) - laccase , chemistry , carboxylic acid , organic chemistry , catalysis , yield (engineering) , alcohol oxidation , alcohol , solvent , aldehyde , enzyme , materials science , metallurgy
Laccase coupled with 2,2,6,6‐tetramethylpiperidinyl‐1‐oxy (TEMPO) is a well‐known catalytic system for the oxidation of alcohols to the carbonyl compounds. In this work, a simple yet effective solvent engineering strategy is developed to enable aromatic alcohols/aldehydes to be efficiently oxidized to carboxylic acids by a laccase‐TEMPO system. Citrate buffer (100–300 m m , pH 6) rather than the widely used acetate buffer (pH 4–5) proves to be optimal for this purpose. The roles of citrate are discussed in laccase‐TEMPO‐catalyzed synthesis of carboxylic acids. 5‐Hydroxymethylfurfural (HMF) of 200 m m is oxidized to 2,5‐furandicarboxylic acid (FDCA), a top‐value biobased chemical in the polymer industry, in 28 h with a yield of up to 97%. Of the 18 substrates examined, 11 alcohols are converted to target carboxylic acids with >90% yields by this method, with 2 alcohols giving >60% yields of carboxylic acids. Gram‐scale preparation of FDCA and 5‐methyl‐2‐pyrazinecarboxylic acid, an important drug intermediate, is demonstrated with total turnover numbers up to 110 000 for laccase and space‐time yields up to 1.0 g/(L•h). This chemoenzymatic approach may be a promising alternative to traditional chemical oxidations for the synthesis of carboxylic acids.