Electronic Supplementary Material (ESI) for Green Chemistry. This journal is © The Royal Society of Chemistry 2021 Supplementary Information Reviving electrocatalytic reductive amination: A sustainable route from biogenic levulinic acid to 1,5-dimethyl-2-pyrrolidone Sonja D. Mürtza, Nils Kuriga, F. Joschka Holzhäusera, Regina Palkovits∗a a Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, 52074 Aachen, Germany. ∗ author of correspondence:
[email protected] Contents Contents 1 Additional results2 1.1 Influence of the amine structure . .2 2 Experimental4 2.1 Electrolysis batch experiments . .4 2.2 Microwave experiments . .5 2.3 Purification of the product solution . .6 2.4 Nuclear magnetic resonance spectroscopy . .6 2.5 Chemicals: Origin and purity . .7 3 NMR spectroscopy8 3.1 Basic equation for calculations . .8 3.2 N-Methylisopropylamine . .9 3.3 N-Methylbutan-2-amine . 10 3.4 N-Methylpentan-2-amine . 11 3.5 N-Methylpentan-3-amine . 12 3.6 N-Methylcyclopentanamine . 13 3.7 4-(Methylamino)-pentanoic acid . 14 3.8 1,5-Dimethyl-2-pyrrolidone . 15 1 1 Additional results 1 Additional results 1.1 Influence of the amine structure Due to the differing results for sterically different ketonic substrates, an impact of the steric hindrance of the amine was expected as well. The reductive amination of acetone with methylamine and ethylamine was already investigated by Smirnov et al.[1] In this work, very similar results were obtained (Figure S1). 1.0 0.8 Conversion Y (Amine) 0.6 Y (Amine)[47] 0.4 Y (Alcohol) Y (Alcohol)[47] 0.2 Conversion, Yield (-) 0.0 Ammonia Methylamine Ethylamine Ethanolamine Figure S1: Conversion and yields Y of the electrocatalytic reductive amination of acetone with different amines compared to the results of Smirnov et al.[1] Conditions: Pb elec- −2 −1 trodes, 0.04 A cm , 2.4 mol L ketone in 0.5 M KH2PO4, acetone to amine ratio: 1:1.2, pH = 12, one faraday equivalent, 283 K.