Affiliation:
1. Corporate Research & Development The Procter & Gamble Company 8700 Mason Montgomery Rd Mason OH 45040
2. Corporate Engineering The Procter & Gamble Company 8256 Union Centre Blvd West Chester Township OH 45069
3. Department of Chemistry & Biochemistry The Ohio State University 100 West 18th Avenue Columbus OH 43210
Abstract
AbstractA 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.