2,2'-Biphenylene phosphorochloridite

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2,2′-Biphenylene phosphorochloridite
Biphenolphosphochloridite.svg
Names
Preferred IUPAC name
6-Chloro-6H-dibenzo[d,f][1,3,2]dioxaphosphepine
Other names
1,1′-Biphenyl-2,2′-diyl phosphorochloridite
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 929-115-2
  • InChI=1S/C12H8ClO2P/c13-16-14-11-7-3-1-5-9(11)10-6-2-4-8-12(10)15-16/h1-8H
    Key: RKNWJMHQLOIGIH-UHFFFAOYSA-N
  • C1=CC=C2C(=C1)C3=CC=CC=C3OP(O2)Cl
Properties
C12H8ClO0P
Molar mass 218.62 g·mol−1
Appearance white solid
Melting point 63 °C (145 °F; 336 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

2,2′-Biphenylene phosphorochloridite is the name for a polycyclic organophosphorus compound with the formula C12H8O2PCl. It is a precursor to diphosphite ligands such as BiPhePhos by reaction with suitable diols. 2,2′-Biphenylene phosphorochloridites, which is a white solid, is prepared from 2,2′-biphenol and phosphorus trichloride. It is prepared by the reaction of 2,2′-biphenol and phosphorus trichloride.[1][2]

References[edit]

  1. ^ Cuny, Gregory D.; Buchwald, Stephen L. (1993). "Practical, High-Yield, Regioselective, Rhodium-Catalyzed Hydroformylation of Functionalized α-Olefins". Journal of the American Chemical Society. 115 (5): 2066–2068. doi:10.1021/ja00058a079.
  2. ^ Van Rooy, Annemiek; Kamer, Paul C. J.; Van Leeuwen, Piet W. N. M.; Goubitz, Kees; Fraanje, Jan; Veldman, Nora; Spek, Anthony L. (1996). "Bulky Diphosphite-Modified Rhodium Catalysts: Hydroformylation and Characterization". Organometallics. 15: 835–847. doi:10.1021/OM950549K.