Reacción #2487424

ord-ce91e59452ea4e858a65cccb183e2524

Ecuación de reacción

C=Cc1ccc(OC(C)(C)C)cc1
p-tert-butoxystyrene
C=CC(=O)OC1CCCCC1
cyclohexyl acrylate
C=CC(=O)OC1CCCCC1.C=Cc1ccc(OC(C)(C)C)cc1
p-tert-butoxystyrene cyclohexyl acrylate

Reactivos

Ninguno

Condiciones de reacción

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

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added to the solution
  2. 2
    Temperaturaafter cooling
  3. 3
    Otroto precipitate the reaction product
  4. 4
    FiltraciónThe precipitated solid was collected by filtration
  5. 5
    Lavadowashed with methanol
  6. 6
    Otrodried under reduced pressure

Procedimiento

176.3, Gram (1.0, mol) of p-tert-butoxystyrene and 16.2 g (0.105, mol) of cyclohexyl acrylate were dissolved in 250 mL of isopropanol and in a nitrogen stream, 2,2′-azobisisobutyronitrile was added to the solution. The resulting mixture was stirred at 75° C. over 6 hours and after cooling, the reaction solution was poured in 5,000 mL of an aqueous methanol solution to precipitate the reaction product. The precipitated solid was collected by filtration, washed with methanol and dried under reduced pressure. In this way, 172.5 g of poly(p-tert-butoxystyrene/cyclohexyl acrylate) was obtained as a white powder crystal.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08795945B2uspto-grants-2014_08