Highly pure a-monoglycerides (5a-e) were successfully prepared in high yields by the condensation of fatty acids such as lauric, myristic, palmitic, stearic and oleic (2a-e) with glycerol carbonate (4-hydroxymethyl-1,3-dioxolan-2-one) (1) in the presence of triethylamine as catalyst. Reaction conditions and spectroscopic identification of products will be presented in this article.
An efficient solvent-free synthesis of a variety of highly pure 1,3-sn-diglycerides (1,3-sn-diacylglycerols) in a two-step one pot process is described. Heating glycerol carbonate (4-hydroxymethyl-1,3-dioxolan-2-one) with fatty acid anhydrides 2a-d affords 1:1 mixtures of glycerol carbonate fatty esters 3a-3d and the corresponding fatty acids. Further heating the reaction mixtures in the presence of catalytic amounts of 1,4-diazabicyclo[2.2.2]octane (DABCO) at 195-200°C yields highly pure 1,3-sn-diglycerides 4a-4d.
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