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High-intensity ultrasound-promoted reformatsky reactions
Nathan A Ross1, Richard A Bartsch
1Department of Chemistry and Biochemistry, Texas Tech University, Lubbock 79409, USA.
The Journal of Organic Chemistry
|January 18, 2003
Abstract:
Reformatsky reactions of a phenyl ketone, an alpha-bromoester, zinc dust, and a catalytic amount of iodine in dioxane under high-intensity ultrasound (HIU) irradiation from an ultrasonic probe give high yields of beta-hydroxyesters in short reaction times. A series of alkyl phenyl ketones with increasing steric demands of the alkyl group are evaluated as potential electrophiles for the reactions with several alpha-bromoesters, also having increasing steric demands. The Reformatsky reaction under HIU is found to be concentration dependent.