تفاعل #2467924

ord-9cf8e8f5e5a54829bd654a608028a9f4

معادلة التفاعل

c1ccc(P(c2ccccc2)c2ccccc2)cc1
Triphenylphosphine
Nc1ccc([N+](=O)[O-])cc1
4-Nitroaniline
O=N[O-].[Na+]
sodium nitrite
O=[N+]([O-])[O-].O=[N+]([O-])c1ccc([PH3+])cc1
4-nitrophenylphosphonium nitrate

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwere prepared by the method of Horner [Chem. Ber. 1958, 91,45] and Rieke [J. Am. Chem. Soc. 1976, 98, 6872]
  2. 2
    workup.ADDITIONwas added
  3. 3
    workup.ADDITIONwas added dropwise
  4. 4
    أخرىthe water layer separated from the ethyl acetate
  5. 5
    استخلاصthe aqueous portion extracted twice with ether
  6. 6
    استخلاصThe ethyl acetate solution was extracted twice with water
  7. 7
    workup.ADDITIONAddition of an aqueous solution of sodium iodide
  8. 8
    أخرىprecipitated the phosphonium iodide, mp 225-227° C. (Lit. 228.5° C.; Chem. Ber. 1958, 91, 45)
  9. 9
    workup.DISSOLUTION4-Nitrophenylphosphonium iodide was dissolved in 5 mL of ethanol
  10. 10
    workup.ADDITIONtreated with an aqueous solution of AgNO3
  11. 11
    أخرىThe silver iodide was removed by filtration
  12. 12
    أخرىthe solution was evaporated to dryness

الإجراء التجريبي

Non-radioactive standards and compounds used for radiolabeling were prepared by the method of Horner [Chem. Ber. 1958, 91,45] and Rieke [J. Am. Chem. Soc. 1976, 98, 6872]. 4-Nitroaniline (2.8 g, 0.02 mol) and the molar equivalent of sodium nitrite were dissolved in 10 ml of concentrated HCl acid 10 ml of water at 0° C. Water (20 ml), in which was dissolved sodium acetate (5.6 g), was added. Triphenylphosphine (5.6 g) dissolved in ethyl acetate (80 ml) was added dropwise with stirring. After one hour, the resulting solution was acidified, the water layer separated from the ethyl acetate, and the aqueous portion extracted twice with ether. The ethyl acetate solution was extracted twice with water, the extracts were combined with the other aqueous fraction. Addition of an aqueous solution of sodium iodide precipitated the phosphonium iodide, mp 225-227° C. (Lit. 228.5° C.; Chem. Ber. 1958, 91, 45). 4-Nitrophenylphosphonium iodide was dissolved in 5 mL of ethanol treated with an aqueous solution of AgNO3. The silver iodide was removed by filtration and the solution was evaporated to dryness. Chromatography of the crude salt on silica gel (methylene chloride/methanol (90:10)) afforded pure 4-nitrophenylphosphonium nitrate; mp 215-127° C. Anal. calcd for C24H19N2O5P: C, 64.57; H, 4.29. Found: C, 64.49; H, 4.14.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08257680B1uspto-grants-2012_09