# Theoretical and Experimental Investigations of Acetal Formation During the Oxidation of Xylose to Formic Acid Catalysed by H5PV2Mo10O40 in Methanolic‐Aqueous Solution

**Authors:** Leon Schidowski, Alexander Buck, Maximilian J. Poller, David Robinson, Jakob Albert

PMC · DOI: 10.1002/cssc.202502661 · Chemsuschem · 2026-03-07

## TL;DR

This study investigates how solvent composition affects the oxidation of xylose to formic acid using a specific catalyst, focusing on the role of acetal formation and reaction intermediates.

## Contribution

The study reveals the importance of solvent composition and reaction conditions in stabilizing intermediates during xylose oxidation catalyzed by H5PV2Mo10O40.

## Key findings

- Acetal formation and esterification are key in protecting reactive functional groups of carbohydrates during oxidation.
- Solvent composition and reaction conditions strongly influence the stability of reaction intermediates.
- DFT calculations highlight the significance of catalyst-solvent interactions over substrate-solvent interactions.

## Abstract

The BioValCat (Enhanced Biomass Valorization by Engineering of Polyoxometalate Catalysts) project aims at developing homogeneously catalysed, selective biomass transformation technologies ultimately leading to an industrial viable biomass valorisation process. Herein, investigations of the conversion pathways for selected model substrates is one of the major tasks. Besides the catalyst‐solvent interactions, the substrate‐solvent interactions also play an important role. In this study, we aimed at answering the fundamental research question: what are the key mechanisms in aqueous‐alcoholic solutions preventing decarboxylation and where are the limits with respect to process conditions and solvent composition? Therefore, a special focus was placed on the influence of the functional groups in different reaction intermediates from HPA‐2 (H5PV2Mo10O40) catalysed xylose oxidation on the way to formic acid. We found that the protection of reactive functional groups of the model carbohydrates depends on the formation and stability of several reaction intermediates, which are formed via acetalization or esterification. This is strongly dependent on solvent composition and reaction conditions. The present findings were supported by DFT‐calculations explaining the different effects of the solvent composition on both substrate and catalyst, emphasising the catalyst‐solvent interactions are of superior importance for catalysis.

The substrate‐solvent interactions play a major role in the modified OxFA process. Herein, the formation and stability of several reaction intermediates via acetalization depending on solvent composition and reaction conditions is investigated.© 2026 WILEY‐VCH GmbH

## Linked entities

- **Chemicals:** xylose (PubChem CID 135191), formic acid (PubChem CID 284)

## Full-text entities

- **Genes:** HPSE2 (heparanase 2 (inactive)) [NCBI Gene 60495] {aka HPA2, HPR2, UFS, UFS1}
- **Chemicals:** PTFE (MESH:D011138), POM (MESH:C000712528), O (MESH:D010100), p (MESH:D010758), hexoses (MESH:D006601), sodium vanadate (MESH:D014638), sugar (MESH:D000073893), acidity (MESH:D000143), FA (MESH:C030544), glycolic acid (MESH:C031149), Methanol (MESH:D000432), T (MESH:D014316), polymer (MESH:D011108), c (MESH:D002244), Acetal (MESH:D000080), hydrazine (MESH:C029424), ester (MESH:D004952), carboxylic acid (MESH:D002264), N2 (MESH:D009584), CO (MESH:D002248), V (MESH:D014639), Glycol aldehyde (MESH:C010972), H2O (MESH:D014867), methyl formate (MESH:C025468), D2O (MESH:D017666), solketal (MESH:C024356), aldehyde (MESH:D000447), hydroxyl radicals (MESH:D017665), EtOH (MESH:D000431), iso-propanol (MESH:D019840), glycerol (MESH:D005990), dimethyl acetal (MESH:C059033), H2O2 (MESH:D006861), Aqueous Hydrazine (-), tert-butanol (MESH:D020002), carbohydrates (MESH:D002241), DMM (MESH:C042581), Xylose (MESH:D014994), chloroform (MESH:D002725), Glyoxal (MESH:D006037), CO2 (MESH:D002245), methylglyoxal (MESH:D011765), dihydroxyacetone (MESH:D004098), argon (MESH:D001128), C1 (MESH:C400149), H2SO4 (MESH:C033158), phosphomolybdic acid (MESH:C003125), ice (MESH:D007053), DMSO (MESH:D004121), Formaldehyde (MESH:D005557), glucose (MESH:D005947), H (MESH:D006859), Mo (MESH:D008982), alcohol (MESH:D000438), Glyceraldehyde (MESH:D005985)
- **Species:** Methylobacillus caricis (species) [taxon 1971611]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12967265/full.md

## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12967265/full.md

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Source: https://tomesphere.com/paper/PMC12967265