AI Article Synopsis

  • * This method is eco-friendly and operates at mild temperatures, contrasting with traditional high-temperature methods that generate complex mixtures.
  • * The dimerization yields valuable products that can be upgraded into bio-jet fuels or other nitrogen-containing chemicals, while minimizing side reactions and allowing for recycling of reactants.

Article Abstract

A simple, solvent-free arginine-catalyzed aldol dimerization of levulinic acid was achieved via the simultaneous formation of a eutectic mixture. Dimers of levulinic acid are valued as biomass-derived fine chemical precursors, with potential to upgrade to bio-jet fuels or N-containing functional chemicals. Typically, these dimers are produced as isomeric mixtures using high temperatures and a variety of solid inorganic catalysts or mineral acids. In this study, an organocatalytic and regioselective dimerization was achieved at 22 % conversion on either a bench or kilogram scale using mild temperatures and only L-arginine as both a co-solvent and catalyst. The intricate H-bonding network comprising the eutectic solvent was harnessed to produce only one product, minimizing side reactivity and preserving the reactants for recycling.

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http://dx.doi.org/10.1002/cssc.202400503DOI Listing

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