Reaktion #2772

ord-a955b85440dc450e8071495d57560dc1

Reaktionsgleichung

CCOC(C)=O
ethyl acetate
C=Cc1ccc(OC(C)(C)C)cc1
p-t-butoxystyrene
CC(C)(C#N)N=NC(C)(C)C#N
azobisisobutyronitrile
O=S(=O)(O)O
sulfuric acid
C#Cc1ccc(O)cc1
poly(p-hydroxystyrene)

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeafter which they were subjected to polymerization for 10 hours under a nitrogen atmosphere while the reaction temperature
  2. 2
    Sonstigewas kept at 80° C
  3. 3
    SonstigeAfter the polymerization
  4. 4
    Sonstigethe resulting mixture was subjected to hydrolysis at 80° C. for 8 hours
  5. 5
    Waschenthe resulting mixture was washed with water
  6. 6
    workup.ADDITIONThe resulting resin solution was dropped into a large amount of water
  7. 7
    SonstigeThe resin was recovered
  8. 8
    Sonstigedried in a vacuum drier

Vorschrift

In 80 g of propylene glycol monomethyl ether was dissolved 88 g of p-t-butoxystyrene, and then, 2 g of azobisisobutyronitrile was added to the solution, after which they were subjected to polymerization for 10 hours under a nitrogen atmosphere while the reaction temperature was kept at 80° C. After the polymerization, an aqueous sulfuric acid solution was added to the reaction mixture and the resulting mixture was subjected to hydrolysis at 80° C. for 8 hours. Subsequently, ethyl acetate was added to the reaction mixture and the resulting mixture was washed with water, after which the solvent was replaced by acetone. The resulting resin solution was dropped into a large amount of water to coagulate a resin. The resin was recovered and dried in a vacuum drier kept at 50° C. overnight to obtain 48 g of a white fine powder of poly(p-hydroxystyrene).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731125uspto-grants-1998_03