An Expeditious Method for the Preparation of 2- Hydroxy-1, 4-dioxane and Its Use in Reductive Alkylation of Amines
2010
Selective oxidation of diethylene glycol by a ruthenium(VIII) species, obtained in situ from ruthenium(III) chloride― sodium periodate in the presence of a catalytic quantity of water, affords a monoaldehyde in the form of the internal acetal 2-hydroxy-1,4-dioxane. This compound was used in reductive alkylations of selected primary and secondary amines, demonstrating its utility in the preparation of target structures with the 2-(2-hydroxy-ethoxy)ethylamino unit.
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