Selective Production of Syringaldehyde and Vanillin from Acetal-Stabilized Lignin

Industrial lignin oxidation has been used for vanillin production but is largely uncontrolled, not fully understood mechanistically, and leads to low yield. Here, we have demonstrated high-efficiency vanillin and syringaldehyde production from lignin via guaiacyl and syringyl α-diketones. These molecules can be selectively produced from lignin, but their valorization has been poorly explored. We therefore explored their conversion into aldehyde equivalents with proven market demand to expand their use. Aryl-α-diketones were hydrogenated to produce the corresponding glycol with a Pt/C catalyst under mild conditions (80 °C, 20 bar H2). This intermediate was then cleaved oxidatively to produce aromatic aldehydes with the VO(acac)2 catalyst using air as the oxidant at 80 °C. Both steps give quantitative yields and are performed in the same solvent (MeTHF) allowing simple processing. By applying this conversion on a stream derived from birch AAF lignin, we were able to produce 4 wt % of aromatic aldehydes on a dry biomass basis.

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Publication Details

Journal
ACS Sustainable Chemistry & Engineering
Published
2025-08-26
DOI
https://doi.org/10.1021/acssuschemeng.5c04387
Primary Topic
Lignin and Wood Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Selective Production of Syringaldehyde and Vanillin from Acetal-Stabilized Lignin

Tom Nelis, Jean Behaghel de Bueren, Irene Martínez-Salazar, Jeremy S. Luterbacher et al.
ACS Sustainable Chemistry & Engineering
Lignin and Wood Chemistry
article

Selective Production of Syringaldehyde and Vanillin from Acetal-Stabilized Lignin

Tom Nelis, Jean Behaghel de Bueren, Irene Martínez-Salazar, Jeremy S. Luterbacher, Romain Fontaine, A. Colantuoni, Wu Lan
article en

Abstract

Industrial lignin oxidation has been used for vanillin production but is largely uncontrolled, not fully understood mechanistically, and leads to low yield. Here, we have demonstrated high-efficiency vanillin and syringaldehyde production from lignin via guaiacyl and syringyl α-diketones. These molecules can be selectively produced from lignin, but their valorization has been poorly explored. We therefore explored their conversion into aldehyde equivalents with proven market demand to expand their use. Aryl-α-diketones were hydrogenated to produce the corresponding glycol with a Pt/C catalyst under mild conditions (80 °C, 20 bar H2). This intermediate was then cleaved oxidatively to produce aromatic aldehydes with the VO(acac)2 catalyst using air as the oxidant at 80 °C. Both steps give quantitative yields and are performed in the same solvent (MeTHF) allowing simple processing. By applying this conversion on a stream derived from birch AAF lignin, we were able to produce 4 wt % of aromatic aldehydes on a dry biomass basis.

ACS Sustainable Chemistry & EngineeringVol. 13(35)
École Polytechnique Fédérale de Lausanne (CH)
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Openalex Percentile: Top 79%
Lignin and Wood Chemistry
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