Specific Organocatalysis in Amidation Reaction of Fatty Acid Methyl Esters with 3‐(Dimethylamino)‐1‐propylamine

Comparison of various organic compounds such as glycols, amines and alkanolamines as organocatalysts in amidation of fatty acid methyl esters with 3‐(dimethylamino)‐1‐propylamine was made for the first time. It was experimentally detected that catalysts containing OH‐groups (alcohols, glycols, glyce...

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Veröffentlicht in:ChemistrySelect (Weinheim) 2021-01, Vol.6 (3), p.480-487
Hauptverfasser: Shirshin, Konstantin K., Esipovich, Anton L., Kazantsev, Oleg A., Rumyantsev, Misha, Korotaev, Mikhail S., Rogozhin, Anton E.
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Sprache:eng
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Zusammenfassung:Comparison of various organic compounds such as glycols, amines and alkanolamines as organocatalysts in amidation of fatty acid methyl esters with 3‐(dimethylamino)‐1‐propylamine was made for the first time. It was experimentally detected that catalysts containing OH‐groups (alcohols, glycols, glycerol and aminoalcohols) influence the reaction rate. Moreover, catalytic effect is depending on the catalysts geometry significantly. 1,5‐diols (e. g. diethylene glycol and diethanolamine) were found to accelerate the reaction more than other OH‐groups containing additives. It was supposed, that this catalytic effect is caused by specific associative interactions between reactants and 1,5‐diols, what was confirmed by quantum mechanics calculations. Catalysts concentration effects on the reaction rate were also investigated. Comparison of various organic compounds such as glycols, amines and alkanolamines as organocatalysts in amidation of fatty acid methyl esters with 3‐(dimethylamino)‐1‐propylamine was made for the first time. It was fixed, that catalytic effect is depending on the catalysts geometry significantly. It was supposed, that this catalytic effect is caused by specific associative interactions between reactants and 1,5‐diols, what was confirmed by quantum mechanics calculations. Catalysts concentration effects on the reaction rate were also investigated.
ISSN:2365-6549
2365-6549
DOI:10.1002/slct.202003197