Реакция #518096

ord-fa3f744e22c74ba58e4a85ae1a5fdd17

Уравнение реакции

C=Cc1ccc(OC(C)(C)C)cc1
p-tert-butoxystyrene
C=Cc1ccc(C(C)(C)C)cc1
p-tert-butylstyrene
CO
methanol
C=Cc1ccc(C(C)(C)C)cc1.C=Cc1ccc(OC(C)(C)C)cc1
p-tert-butoxystyrene p-tert-butylstyrene

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеprecipitated resin
  2. 2
    Другоеthe resultant was dried under reduced pressure

Методика

With the use of 100 g (0.567 mole) of p-tert-butoxystyrene and 5.3 g (0.03 mole) of p-tert-butylstyrene, the same polymerization reaction and after-treatment as described in Production Example 2-(1) were conducted. Then, the resulting viscous resinous material was dissolved in 300 g of acetone and poured into 2000 ml of 50% aqueous methanol solution and precipitated resin was subjected to decantation. This process step was conducted further twice, and the resultant was dried under reduced pressure to give 94.5 g of poly(p-tert-butoxystyrene/p-tert-butylstyrene) as white powders. Then, 70 g of the polymer was subjected to the same reaction and after-treatment as described in Production Example 9-(1) to give 48.5 g of poly(p-hydroxystyrene/p-tert-butylstyrene) as white powders. A ratio of p-hydroxystyrene unit and p-tert-butylstyrene unit was about 94:6 by 1HNMR. Mw: about 16000, Mw/Mn: 1.29 (GPC method: polystyrene as standard).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06656660B1uspto-grants-2003_12