© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim The hydrocarboxylation of allyl cyanide with monodentate phosphine systems (Pd/triphenylphosphine and protic acid cocatalyst) gave branched 3-cyano-2-methylpropanoic acid chemo- and regioselectively, whereas with bidentate systems (Pd/bis[(2-diphenylphosphino)phenyl] ether and protic acid cocatalyst) it gave linear 4-cyanobutanoic acid chemo- and regioselectively. 3-Cyano-2-methylpropanoic acid and 4-cyanobutanoic acid were isolated in high yields as carboxylic acids and purified as benzyl esters. No isomerization of allyl cyanide to crotononitrile or its carbonylated derivatives was observed in any case. In parallel experiments, deuterocarboxylation under the same conditions gave the corresponding deuterated products, which were analyzed by MS and 2H NMR spectroscopy: only d0, d1, and d2 products were detected. Deuterium entered the β and γ-CN positions of the products but never the α position.
- homogeneous catalysis
- isotopic labeling
Vallcorba, O., Polo, A., & Real, J. (2017). Selective Catalytic Hydrocarboxylation and Deuterocarboxylation of Allyl Cyanide to Cyanobutanoic Acids with Monodentate and Bidentate Phosphines. ChemCatChem, 9(6), 1105-1112. https://doi.org/10.1002/cctc.201601436