Réaction #324371

ord-fd69cfff23654517bbdcb8f85511322a

Équation de réaction

CO
methanol
C=Cc1ccc(OC(C)(C)C)cc1
p-tert-butoxystyrene
C=CC(=O)OC1CCCCC1
cyclohexyl acrylate
CC(C)(C#N)N=NC(C)(C)C#N
2,2′-azobisisobutyronitrile
C=CC(=O)OC1CCCCC1.C=Cc1ccc(OC(C)(C)C)cc1
p-tert-butoxystyrene cyclohexyl acrylate

Conditions de réaction

Température
75°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reaction liquid
  2. 2
    Températurewas cooled
  3. 3
    Autreprecipitating a reaction product
  4. 4
    FiltrationThe precipitated solid was collected by filtration
  5. 5
    Lavagewashed with methanol
  6. 6
    Autredried in vacuum

Mode opératoire

First, 176.3 g (1.0 mol) of p-tert-butoxystyrene and 16.2 g (0.105 mol) of cyclohexyl acrylate were dissolved in 250 ml of isopropanol. In a nitrogen stream, 2,2′-azobisisobutyronitrile was added to the solution, and agitated at 75° C. for six hours. The reaction liquid was cooled, and poured in 5000 ml of an aqueous solution of methanol, thereby precipitating a reaction product. The precipitated solid was collected by filtration, washed with methanol, and dried in vacuum. Thus, 172.5 g of poly(p-tert-butoxystyrene/cyclohexyl acrylate) was obtained as a white powdery crystal.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08642245B2uspto-grants-2014_02