Microwave-Assisted Synthesis of Vinyl Esters through Ruthenium-Catalyzed Addition of Carboxylic Acids to Alkynes
François Nicks A , Lionel Libert A , Lionel Delaude A and Albert Demonceau A BA Laboratory of Macromolecular Chemistry and Organic Catalysis, University of Liège, Sart-Tilman (B.6a), B-4000 Liège, Belgium.
B Corresponding author. Email: a.demonceau@ulg.ac.be
Australian Journal of Chemistry 62(3) 227-231 https://doi.org/10.1071/CH08480
Submitted: 3 November 2008 Accepted: 19 December 2008 Published: 20 March 2009
Abstract
A rapid and efficient method is described for the selective synthesis of enol esters via the microwave-accelerated addition of carboxylic acids to terminal alkynes. The method employs the readily available [RuCl2(p-cymene)(PPh3)] complex as catalyst without the need of bases, and reactions are complete in 20 min.
Acknowledgements
The authors thank the ‘Fonds pour la Formation à la Recherche dans l’Industrie et dans l’Agriculture’ (FRIA) for a fellowship to F. Nicks and the ‘Fonds National de la Recherche Scientifique’ (FNRS), Brussels, for financial support of the present work (grants FRFC 2.4565.07 and 2.4645.07) and for the purchase of major instrumentation. We also thank BRS, Drogenbos, Belgium, for helpful discussion and technical support.
[1]
(a) A. Demonceau,
A. W. Stumpf,
E. Saive,
A. F. Noels,
Macromolecules 1997, 30, 3127.
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