Hydrogen Methyl Phenylphosphonate置于sodium Periodate,Benzotriazol-1-Yloxyl-Tris-(Pyrrolidino)-Phosphonium Hexafluorophosphate,N,N-二异丙基乙胺体系中,用 1,4-二氧六环,N,N-二甲基甲酰胺 用作溶剂,化学反应 13.0H,反应生成苯基膦酸二甲酯
参考文献:(1H-Benzotriazol-1-Yloxy)Tris(Dimethylamino)Phosphonium Hexafluorophosphate-And (1H-Benzotriazol-1-Yloxy)Tripyrrolidinophosphonium Hexafluorophosphate-Mediated Activation Of Monophosphonate Esters: Synthesis Of Mixed Phosphonate Diesters,The Reactivity Of The Benzotriazolyl Phosphonic Esters Vs The Reactivity Of The Benzotriazolyl Carboxylic Esters
标题:(1H-Benzotriazol-1-Yloxy)Tris(Dimethylamino)Phosphonium Hexafluorophosphate-And (1H-Benzotriazol-1-Yloxy)Tripyrrolidinophosphonium Hexafluorophosphate-Mediated Activation Of Monophosphonate Esters: Synthesis Of Mixed Phosphonate Diesters,The Reactivity Of The Benzotriazolyl Phosphonic Esters Vs The Reactivity Of The Benzotriazolyl Carboxylic Esters
摘要:A General Method For Synthesizing Mixed Phosphonate Diesters From Monoesters Using (1H-Benzotriazol-1-Yloxy)Tris(Dimethylamino) Hexafluorophosphate Or (1H-Benzotriazol-1-Yloxy)Tripyrrolidinophosphonium Hexafluorophosphate Reagents Is Described. The Reaction Proceeded Through A Benzotriazolyl Ester As Shown By Comparison With Other Reagents Such As Dcc,Dcc/dmap,Dcc/1-Hydroxybenzotriazole,Bromotris(Dimethylamino)Phosphonium Hexafluorophosphate,Or O-(1H-Benzotriazol-1-yl)-N,N,N',N'-Tetramethyluronium Hexafluorophosphate And By P-31 NMR Analysis. This Benzotriazolyl Phosphonic Ester Intermediate Was More Reactive Toward Alcohols Than Toward Amines,Contrary To Its Carboxylic Analogue.
Doi:10.1021/jo00121A045