4.6 Article

Highly regioselective hydroaminomethylation of long chain alkenes catalyzed by Rh-BISBIS in a two-phase system

Journal

CATALYSIS COMMUNICATIONS
Volume 7, Issue 12, Pages 979-981

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.catcom.2006.04.010

Keywords

hydroaminomethylation; long chain alkene; Rh complex; aqueous two-phase catalysis

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The hydroaminomethylation of long chain alkenes with secondary amines in aqueous/organic two-phase system catalyzed by rhodium catalyst precursor and water-soluble diphosphine ligand BISBIS (sulfonated 2,2'-bis(diphenylphosphinomethyl)-1,1'-biphenyl) was investigated. The result showed that the use of BISBIS improved the reaction activity and especially regioselectivity for linear amine significantly compared with the monophosphine ligand TPPTS [P(m-C6H4SO3Na)(3)] the ratio of linear to branched amine was up to 83. (c) 2006 Elsevier B.V. All rights reserved.

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