Synthesis of [ 13C]- and [ 14C]-labeled phenolic humus and lignin monomers

Abstract

Natural phenolic monomers are ubiquitous in the environment and are involved in the stabilization of atmospheric carbon and the transformation of xenobiotics. Investigations on the stabilization of phenolic carbons and their environmental fate are hampered by the unavailability of commercial [ 13C]- and [ 14C]-labeled phenols. Here we report the complete chemical synthesis of the lignin and humus structural monomers p-coumaric, ferulic, and caffeic acids, p-hydroxybenzaldehyde, protocatechualdehyde, vanillin, catechol, and guaiacol, uniformly [ 13C]- or [ 14C]-labeled in the aromatic ring, starting from commercially available [U-ring- 13C]- or [U-ring- 14C]-labeled phenol. The synthesis of these compounds involved selective ortho-hydroxylation of the aromatic ring, Friedel–Crafts alkylation, and Knoevenagel condensation. [U-ring- 13C]- or [U-ring- 14C]- p-coumaric acid was synthesized via p-hydroxybenzaldehyde with a 75% yield with respect to phenol. Synthesis of [U-ring- 13C]- or [U-ring- 14C]-ferulic acid, consisting of six single steps via guaiacol and vanillin, had an overall yield of up to 45%. Uniformly ring-labeled caffeic acid was synthesized either via catechol and protocatechualdehyde in five single steps, yielding [U-ring- 14C]-caffeic acid with a 37% yield, or via guaiacol, vanillin, and ferulic acid in seven steps, yielding [U-ring- 13C]-caffeic acid with an 18% yield. Ferulic acid, [ 14C]-labeled at β-C of the propenoic side chain, was synthesized from [2- 14C]-malonic acid under Knoevenagel conditions with a 67% yield with respect to malonic acid. Demethylation of the [β- 14C]-ferulic acid with BBr 3 in CH 3CN resulted in [β- 14C]-caffeic acid with a 62% yield. All [U-ring- 13C]-labeled phenolic products were analyzed by 13C nuclear magnetic resonance ( 13C-NMR) spectroscopy and gas chromatography–mass spectrometry (GC–MS).