Reactions of alkenes and alkynes with formaldehyde catalyzed by rhodium systems containing phosphine ligands

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Abstract

The reaction of alkenes (allyl alcohol, styrene and C6 alkenes) with formaldehyde was efficiently performed by using Rh precatalysts formed in situ by the addition of triphenylphosphine (PPh3), 1,2-bis(diphenylphosphino)ethane (dppe) or 1,1,1-tris(diphen-ylphosphinomethyl)ethane (triphos) to the complex Rh(acac)(CO)2 at 130ºC in 1,4-dioxane, yielding their corresponding aldehydes; the best catalytic system was Rh(acac)(CO)2/2dppe, which generates the cationic complex [Rh(k2-P,P-dppe)2]+. However, the reaction of pheny-lacetylene with formaldehyde under the same reaction conditions generated styrene, which was found to be the product of transfer hydrogenation from formaldehyde.

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Rosales, M., González, B., Molina, J., Pérez, H., Modroño-Alonso, M., & Baricelli, P. J. (2017). Reactions of alkenes and alkynes with formaldehyde catalyzed by rhodium systems containing phosphine ligands. Journal of the Mexican Chemical Society, 61(2), 120–127. https://doi.org/10.29356/jmcs.v61i2.259

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