Reacción #324371

ord-fd69cfff23654517bbdcb8f85511322a

Ecuación de reacción

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

Condiciones de reacción

Temperatura
75°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction liquid
  2. 2
    Temperaturawas cooled
  3. 3
    Otroprecipitating a reaction product
  4. 4
    FiltraciónThe precipitated solid was collected by filtration
  5. 5
    Lavadowashed with methanol
  6. 6
    Otrodried in vacuum

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08642245B2uspto-grants-2014_02