Reaktion #162259

ord-ca6eee362d3d46539288822cee8c8317

Reaktionsgleichung

C=CP(=O)(O)O
vinylphosphonic acid
C=CC(N)=O
acrylamide
CC(C)(C#N)N=NC(C)(C)C#N
AIBN
C=CC(N)=O.C=CP(=O)(O)O
Vinylphosphonic Acid Acrylamide

Lösungsmittel

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeIn a 10 liter flask equipped with a stirrer
  2. 2
    workup.ADDITIONthe obtained solution was added dropwise in a reactor over 4 hours
  3. 3
    workup.ADDITIONDuring the dropwise addition of a monomer solution
  4. 4
    Sonstigea white precipitate was produced
  5. 5
    TemperaturAfter heating
  6. 6
    Temperaturwhile maintaining at 70° C.
  7. 7
    Temperaturheating
  8. 8
    Temperaturthe reaction solution was cooled to room temperature
  9. 9
    SonstigeThe precipitate thus produced
  10. 10
    Filtrationwas collected by filtration under reduced pressure
  11. 11
    Waschenwashed with 1,000 g of ethanol
  12. 12
    SonstigeThe precipitate was vacuum-dried at 40° C. for 24 hours
  13. 13
    Sonstigeto obtain a white fine crystal

Vorschrift

In a 10 liter flask equipped with a stirrer, a capacitor and a dropping device, 3,500 g of ethanol was charged and heated to 70° C. Then, 720 g (6.67 mol) of a vinylphosphonic acid monomer, 880 g (12.38 mol) of acrylamide and 52 g of AIBN were dissolved in 1,000 g of ethanol and the obtained solution was added dropwise in a reactor over 4 hours. During the dropwise addition of a monomer solution, a white precipitate was produced. After heating and stirring for 2 hours while maintaining at 70° C., heating was stopped and the reaction solution was cooled to room temperature. The precipitate thus produced was collected by filtration under reduced pressure and then washed with 1,000 g of ethanol. The precipitate was vacuum-dried at 40° C. for 24 hours to obtain a white fine crystal. Yield: 1,550 g

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08835099B2uspto-grants-2014_09