4-Ethenylphenyl acetate → p-Acetyloxystyrene p-tert-butoxystyrene

HRID 1600505Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1600505
[C:1]([O:4][C:5]1[CH:12]=[CH:11][C:8]([CH:9]=[CH2:10])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].[C:13]([O:17][C:18]1[CH:25]=[CH:24][C:21]([CH:22]=[CH2:23])=[CH:20][CH:19]=1)([CH3:16])([CH3:15])[CH3:14].N(C(C)(C(C)C)C#N)=NC(C)(C(C)C)C#N>>[C:13]([O:17][C:18]1[CH:19]=[CH:20][C:21]([CH:22]=[CH2:23])=[CH:24][CH:25]=1)([CH3:16])([CH3:14])[CH3:15].[C:1]([O:4][C:5]1[CH:12]=[CH:11][C:8]([CH:9]=[CH2:10])=[CH:7][CH:6]=1)(=[O:3])[CH3:2]

Komponenten

4

Versuchsvorschrift

Using 48.6 g (0.3 mol) of p-acetyloxystyrene, 17.6 g (0.1 mol) of p-tert-butoxystyrene and a catalytic amount of 2,2'-azobis(2-methylisovaleronitrile), the procedure of (1) of Preparation Example 3 was carried out for reaction and after-treatments to obtain 59.7 g of poly(p-tert-butoxystyrene/p-acetyloxystyrene) as white powdery crystal. P-acetyoxystyrene unit/p-tert-butoxystyrene unit molar ratio in the polymer≈3:1 (1NMR). Mw≈10,500; Mw/Mn=1.32 (GPC with polystyrene calibration).

Aufarbeitung

  1. customwas carried out for reaction

Quellen und Nachweise

ORD-Eintrag
ord-8e92069560ec4ad3a8a656fc8057ab19
Quelldatensatz
uspto-grants-1999_11
Patentnummer
US05976759

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