The Palladium-Catalyzed Carboxytelomerization of Butadiene with Agrobased Alcohols and Polyols
Emma Wilson1, Clément Dumont2, Mathieu Drelon1
1Université de Lille, CNRS, Centrale Lille, Ecole Nationale Supérieure de Chimie de Lille (ENSCL), Université d'Artois, Unité de Catalyse et Chimie du Solide (UCCS)-UMR 8181, F-59000, Lille, France.
Abstract:
The palladium catalyzed carboxytelomerization reaction of alcohols with butadiene allows for efficient and atom-economical access to unsaturated alkyl nona-3,8-dienoate esters. The study focused on the nature of the catalyst (phosphine and acid) with ethanol. Commercially available triarylphosphines and carboxylic acids associated with a simple palladium precursor appear to be the best combination for in situ generation of the catalyst. The reaction conditions were further optimized and the carboxytelomerization reaction was efficiently applied to the full transformation of several industrially relevant agro-based monoalcohols and polyols.
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