The synthesis of carboxylica cids is of fundamental importance in the chemical industry and the corresponding products find numerous applications for polymers,c osmetics, pharmaceuticals,a grochemicals,a nd other manufactured chemicals.A lthough hydroxycarbonylations of olefins have been knownf or more than 60 years,c urrently knownc atalyst systems for this transformation do not fulfill industrial requirements,for example,stability.Presented herein for the first time is an aqueous-phase protocol that allows conversion of various olefins,including sterically hindered and demanding tetra-, tri-, and 1,1-disubstituted systems,aswell as terminal alkenes,into the corresponding carboxylic acids in excellent yields.T he outstanding stability of the catalyst system (26 recycling runs in 32 days without measurable loss of activity), is showcased in the preparation of an industrially relevant fatty acid. Key-tosuccess is the use of abuilt-in-base ligand under acidic aqueous conditions.This catalytic system is expected to provide abasis for new cost-competitive processes for the industrial production of carboxylic acids.