Tandem Hydrogenation and Hydrolytic Ring-Opening of Benzofurans to Hydroxyalkyl-Substituted Cyclohexanols Catalyzed by Supported Ruthenium Nanoparticles
Abstract A new synthetic route toward 1,2-hydroxyalkyl-substituted cyclohexanols via catalytic tandem hydrogenation–hydrolytic ring-opening of benzofurans in water is reported. Catalysts based on Ru nanoparticles immobilized on a hydrothermally-stable supported ionic liquid phase (Ru@SILPAC) enable the conversion of benzofuran derivatives into valuable polyols (40–68% isolated yields) using hydrogen and water as the only reactants. Mechanistic investigations identify 2,3-dihydrobenzofuran as a key intermediate, consistent with a sequential pathway involving partial hydrogenation followed by hydrolytic ring opening. The Ru@SILPAC catalyst is recyclable and exhibits high stability under hydrothermal conditions. This work introduces a new transformation of benzofurans and provides a catalytic route to oxygenated carbocyclic scaffolds in line with green chemistry principles.
Authors
- Neha Antil (ORCID: https://orcid.org/0000-0002-2829-8932)
- Walter Leitner (ORCID: https://orcid.org/0000-0001-6100-9656)
- Alexis Bordet (ORCID: https://orcid.org/0000-0003-0133-3416)
- Bhaskar Paul (ORCID: https://orcid.org/0000-0002-5097-7157)
- Vishrant Kumar (ORCID: https://orcid.org/0009-0008-4998-0165)
- Daniela Sorokin
Institutions
- Max Planck Institute for Chemical Energy Conversion (DE)
- RWTH Aachen University (DE)
Publication Details
- Journal
- ACS Sustainable Chemistry & Engineering
- Published
- 2026-09-25
- DOI
- https://doi.org/10.1021/acssuschemeng.6c06467
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00