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Synthesis of Monoalkyl Glyceryl Ethers by Ring Opening of Glycidol with Alcohols in the Presence of Lewis Acids.

ChemSusChem (2016-11-24)
Raffaele Cucciniello, Maria Ricciardi, Rosa Vitiello, Martino Di Serio, Antonio Proto, Carmine Capacchione
RESUMEN

The present work deals with the production of monoalkyl glyceryl ethers (MAGEs) through a new reaction pathway based on the reaction of glycidol and alcohols catalyzed by Lewis acid-based catalysts. Glycidol is quantitatively converted with high selectivity (99 %) into MAGEs under very mild reaction conditions (80 °C and 0.01 mol % catalyst loading) in only 1 h using Al(OTf)

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Sigma-Aldrich
Zinc trifluoromethanesulfonate, 98%
Sigma-Aldrich
Glicidol, 96%
Sigma-Aldrich
Bismuth(III) trifluoromethanesulfonate
Sigma-Aldrich
Iron(III) trifluoromethanesulfonate, 90%