| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 67561 | Journal of Molecular Catalysis A: Chemical | 2008 | 9 Pages |
A simple and efficient procedure is described for the synthesis of 2,6- and 3,6-heptadienoic acids and allyl esters consisting of Rh-catalyzed coupling of but-3-enoic acid and allyl derivatives such as allyl bromide, allyl acetate, and allyl methyl carbonate in alkaline water or in alkaline water/organic two-phase systems. 2,6-Heptadienoate derivatives are the main products in water as acids and in biphasic systems as acids and allyl esters. The latter can be selectively obtained via one-pot cascade esterification reaction using allyl bromide in biphasic systems. The nature of organic solvent, the base concentration and the addition of triphenylphosphine (TPP) in biphasic media allow to tune the regioselectivity of the reaction towards 3,6- or 2,6-derivatives. Substituted but-3-enoic acids and allyl bromides, and pent-4-enoic acid led to moderate or poor results.
Graphical abstractAn effective rhodium-catalyzed procedure for the synthesis of 2,6- and 3,6-heptadienoic acids and their allyl esters is described. Combinations of different allyl substrates with various alkaline aqueous–organic two-phase systems and the presence of a phosphinic ligand allowed tuning the regioselectivity with regard to the 2,6- or 3,6-heptadienoic derivative formation and the chemoselectivity with regard to the heptadienoic acids or allyl esters. Figure optionsDownload full-size imageDownload as PowerPoint slide
