Publication | Open Access
Glycolaldehyde as a Bio-Based C<sub>2</sub> Platform Chemical: Catalytic Reductive Amination of Vicinal Hydroxyl Aldehydes
61
Citations
40
References
2019
Year
Toxic Ethylene OxideBioorganic ChemistryEngineeringMethanolOrganic ChemistryChemistryChemical EngineeringGlycosylationIndustrial CatalysisVicinal Hydroxyl AldehydesBiocatalysisSmallest Sugar MoleculeCatalysisCatalytic SynthesisBiomolecular EngineeringCatalytic Reductive AminationNatural SciencesReductive AminationMolecular CatalysisChemical Kinetics
Reductive amination of glycolaldehyde (GA), the smallest sugar molecule and obtainable from biomass, creates a versatile platform for ethylamine products, potentially replacing current pathways via toxic ethylene oxide and dichloroethane. Given the high reactivity of α-OH carbonyls, the main challenge was control of selectivity in a cascade of parallel and consecutive reactions during reductive amination. The type of solvent and catalyst, preferably methanol and Pd, respectively, are key enabling parameters to achieve high product yields. A kinetic study on product intermediates accompanied with detailed product analysis (MS and NMR) suggested a general mechanistic scheme and validation with density functional theory calculations provided a rational understanding of the solvent effect in terms of energetics and kinetics. Primary alkanolamines (AA) such as 2-(dimethylamino)-ethanol are preferred products, and large excess of the amine reagent is not required to reach almost quantitative yields. Interestingly substoichiometric amine-to-GA ratio allows for high yield of higher (consecutive) AAs such as N-methyldiethanolamine (MDEA) and triethanolamine, for which a peculiar cyclic 5-membered oxazolidinic precursor was analyzed (e.g., for reaction with monomethylamine to MDEA). The shift to diamine-selective (DA) reactions is possible by switching to a two-step one-pot approach. With ethylene glycol as a preferred solvent, high yield of an unsaturated C2-ene-diamine precursor is obtained under an inert atmosphere, followed by its metal-catalyzed hydrogenation at elevated temperature to the final DA product such as N,N,N′,N′-tetramethylethylene-diamine. A conceptual model of the catalytic reductive amination routes that allows production of a variety of ethylamines with up to +90 C % yield is thus presented. The successful preparation and sensory assessment of a GA-based diester quat in fabric softener formulations demonstrates the viability of a full bio-based and drop-in production route for high-value chemicals, directly from GA as a platform molecule.
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