Bulletin of the Chemical Society of Japan · 1981 · 20 citations · 4 references
Natural SciencesChemical EngineeringChemistryCatalysisOrganic ChemistryReaction EngineeringCatalyst DesignCatalyst PreparationCatalyst SynthesisCatalytic MaterialsCatalytic MechanismsOrganic SynthesisAldehydesCatalyst MechanismsCatalyst Structure - Activity RelationshipsCatalytic Reaction MechanismsKetonesOrganic Reaction ChemistryOrganic Reaction MechanismsWater-gas Shift Reaction
Abstract The hydrocarbonylation of propene with CO and H2O to give dipropyl ketones occurs predominantly over forming C4-aldehydes; the catalyst solutions employed are prepared in situ from Co2(CO)8, various phosphines as ligands, and H2O, a high molar ratio of propene to Co2(CO)8 of 300/2 being required. Of the several phosphorus ligands examined, 1,2-bis(diphenylphosphino) ethane (diphos) and bis(diphenylphosphino) acetylene are relatively effective for the formation of the ketones (abbreviated as [ketones]). The effects of the reaction variables (CO pressure, temperature, and H2O concentration) on [ketones] are also examined using the Co2(CO)8–diphos system; [ketones] increases with the initial increase in CO pressure, but reaches a maximum at ca. 100 kg/ cm2 and decreases thereafter. Pronounced decreases of [ketones] are observed when pyridine as well as hydrogen is added to the catalyst solutions.
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Formation of Ketones in the Oxo Synthesis
J. A. Bertrand, Clyde L. Aldridge, Steinar Husebye et al. · The Journal of Organic Chemistry · 1964 · 31 citations