14848-71-6Relevant articles and documents
Tf2O/DMSO-Promoted P-O and P-S Bond Formation: A Scalable Synthesis of Multifarious Organophosphinates and Thiophosphates
Shen, Jian,Li, Qi-Wei,Zhang, Xin-Yue,Wang, Xue,Li, Gui-Zhi,Li, Wen-Zuo,Yang, Shang-Dong,Yang, Bin
supporting information, p. 1541 - 1547 (2021/04/05)
A Tf2O/DMSO-based system for the dehydrogenative coupling of a wide range of alcohols, phenols, thiols, and thiophenols with diverse phosphorus reagents has been developed. This metal- and strong-oxidant-free strategy provides a facile approach to a great variety of organophosphinates and thiophosphates. The simple reaction system, good functional-group tolerance, and broad substrate scope enable the application of this method to the modification of natural products and the direct synthesis of bioactive molecules and flame retardants.
Electrochemical Dehydrogenative Coupling of Alcohols with Hydrogen Phosphoryl Compounds: A Green Protocol for P?O Bond Formation
Li, Qian-Yu,Swaroop, Toreshettahally R.,Hou, Cheng,Wang, Zi-Qiang,Pan, Ying-Ming,Tang, Hai-Tao
supporting information, p. 1761 - 1765 (2019/02/20)
This study reports the environment-friendly electrochemical transformation of structurally diverse phosphorus compounds and alcohol into phosphonates in the presence of ammonium iodide as electrolyte and redox catalyst in acetonitrile at ambient temperature. This method for P?O bond formation exhibits remarkable features, such as transition metal- and oxidant-free conditions. A reliable mechanism is proposed after control and cyclic voltammetry experiments. (Figure presented.).
Hydrolysis of a monocyclic oxyphosphorane containing a five-membered ring
McGall, Glenn H.,McClelland, Robert A.
, p. 2075 - 2083 (2007/10/02)
A kinetic study is reported for the hydrolysis of 2,2-diphenyl-2-methoxy-1,3,2-dioxaphospholane 1.This phosphorane exists in aqueous solution in a pseudo acid-base equilibrium with observable phosphonium ion, the ring-opened (2'-hydroxyethoxy)diphenylmethoxyphosphonium ion 5.The equilibrium constant Ka (+>/) is 9*10-9, values determined by kinetic and spectroscopic methods being in good agreement.This phosphonium ion is, however, not involved in the overall hydrolysis reaction, which proceeds via the thermodynamically less stable cyclic five-membered phosphonium ion derived by loss of the exocyclic methoxy group from the phosphorane, the 2,2-diphenyl-1,3,2-dioxaphospholan-2-ylium ion 6.This route for the overall hydrolysis is established by analysis of the products, and by the observation that the rate constant for the dissappearance of 5 in acid solutions is 40000 times greater than that for an analog that differs only in not being able to cyclize, the (2'-methoxyethoxy)diphenylmethoxyphosphonium ion 7.At all pH, the phosphorane 1 and the ring-opened phosphonium ion 5 exist in equilibrium, and the rate-limiting step in the overall hydrolysis is the cleveage of the exocyclic methoxy group to give the cyclic phosphonium ion 6, which is rapidly converted to products by reaction with water.The actual equilibration reaction involving 1 and 5 cannot be observed at any pH, even with stopped-flow spectroscopy.The non-catalyzed ring clusore of the phosphonium ion 5 reforming the phosphorane 1 occurs with a rate constant of 200-500 s-1, corresponding to an effective molarity of (2-5)*107M for the intramolecular hydroxy group in this reaction.The rate-limiting exocyclic cleavage is assisted by H+, with a very large rate constant 2*109 M-1 s-1.Catalysis by general acids is also observed.The Broenstedt plot has a slope α of 1.0 for weaker acids, with a break for acids with pKa3.This "Eigen"-type behaviour is proposed to arise from a transition state with little phosphonium ion character, in which the proton is almost completely transferred for the weaker acids. Key words: phosphorane, phosphate, phosphonium, hydrolysis.
