Réaction #324372

ord-768308e183ad4759820f49c6b12460b0

Équation de réaction

C=CC(=O)OC1CCCCC1.C=Cc1ccc(OC(C)(C)C)cc1
p-tert-butoxystyrene cyclohexyl acrylate
Cl
hydrochloric acid
C=CC(=O)OC1CCCCC1.C=Cc1ccc(O)cc1
p-hydroxystyrene 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 water
  6. 6
    Autredried in vacuum

Mode opératoire

Next, 130.5 g of poly(p-tert-butoxystyrene/cyclohexyl acrylate) was suspended in isopropanol. Subsequently, 30 ml of concentrated hydrochloric acid was added to the suspension, and agitated at 70 to 80° C. for four hours. The reaction liquid was cooled, and poured in 1500 ml of water, thereby precipitating a reaction product. The precipitated solid was collected by filtration, washed with water, and dried in vacuum. Thus, 85.5 g of poly(p-hydroxystyrene/cyclohexyl acrylate) was obtained as a white powdery crystal.

Source

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