Citation:
YU Hongwei, GUAN Min, TONG Qingsong, JIA Li, JIN Zilin, SHI Jicheng. Synthesis and Enhanced Activity of Etherlized Ferrocenylphosphine for the PalladiumCatalyzed Suzuki Reaction[J]. Chinese Journal of Applied Chemistry,
;2011, 28(8): 887-891.
doi:
10.3724/SP.J.1095.2011.00541
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A new etherlized ferrocenylphosphine ligand,2-diphenylphosphino-ferrocenyl-ethyl-5-hydroxyl-3-oxo-pentyl ether,was prepared by the reaction of acetyl 1-(diphenylphosphinoferrocenyl) ethyl ester with diethylene glycol in 77% yield.Its structure was characterized by 1H NMR,13C NMR,31P NMR and MS.The synthesized ferrocenylphosphine has been applied as supporting ligand in the palladium-catalyzed Suzuki reaction;its ligated palladium catalyst is effective for coupling a range of aryl bromides as well as aryl chlorides having electron-withdrawing groups with phenylboronic acid to prepare the corresponding biaryls.The possible coordination of ether-oxygen to the Pd center may enhance the catalytic performance of the ligand for cross-coupling reaction.
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Keywords:
- ferrocenylphosphine,
- etherlization,
- palladium,
- Suzuki reaction,
- biaryl
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