64091-23-2Relevant articles and documents
IX. Mono- and biphasic asymmetric hydroformylation with rhodium catalysts of the diphosphine ligand NAPHOS and its sulfonated derivatives
Eckl, Robert W.,Priermeier, Thomas,Herrmann, Wolfgang A.
, p. 243 - 249 (2007/10/03)
Both enantiomers of the diphosphine 2,2′-bis(diphenylphosphinomethyl)-1,1′-binaphthyl NAPHOS were prepared by resolution of the racemic P,P′-dioxide and subsequently applied in the rhodium-catalyzed, asymmetric hydroformylation of styrene. Optically active, highly water-soluble derivatives BINAS were prepared by direct sulfonation of the enantiopure diphosphine NAPHOS and applied in aqueous/organic, two-phase hydroformylation of styrene. The catalytically active rhodium complexes HRh(CO)2(P-P) of both NAPHOS and BINAS were prepared and characterized by infrared and NMR spectroscopy. Optical yields are lower in two-phase hydroformylation compared with the conventional single-phase (organic solvent) technique.
Binas - Synthesis and use of a new ligand for propylene hydroformylation
Bahrmann, Helmut,Bergrath, Klaus,Kleiner, Hanss-Jerg,Lappe, Peter,Naumann, Christoph,Peters, Dieter,Regnat, Dieter
, p. 97 - 100 (2007/10/03)
BINAS is a new, very efficient ligand for propylene hydroformylation. BINAS is made by the sulfonation of NAPHOS. Different synthetic routes to NAPHOS are discussed. A new two step synthesis starting from 2,2′-bis(bromomethyl)-1,1′-binaphthyl is described.