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Variation in the regioselectivity of levulinic acid bromination in ionic liquids
Authors:Alexander G. Zavozin  Natalya E. Kravchenko  Sergei G. Zlotin
Affiliation:a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences (ZIOC RAS), 47 Leninsky prosp., Moscow 119991, Russia
b Merck KGaA, Frankfurter Strasse 250, D-64293 Darmstadt, Germany
Abstract:
The reaction of levulinic acid and its esters with bromine in ionic liquids results in the formation of 3-bromo derivatives as the major products and not the 5-bromo substituted isomers, which are typically formed in organic solvents. The bromination of levulinic acid in ionic liquids in the presence of urea leads to the formation of 5-bromolevulinic acid.
Keywords:Levulinic acid   Bromination   Regioisomers   Ionic liquids
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