4-Vinylphenol → p-(1-Ethoxyethoxy)styrene p-hydroxystyrene p-tert-butoxystyrene

HRID 743939

Reaktionsgleichung

Reaktionsgleichung von HRID 743939
[CH2:1]([O:3][CH:4]([O:6][C:7]1[CH:14]=[CH:13][C:10]([CH:11]=[CH2:12])=[CH:9][CH:8]=1)[CH3:5])[CH3:2].[OH:15][C:16]1[CH:23]=[CH:22][C:19]([CH:20]=[CH2:21])=[CH:18][CH:17]=1.[C:24]([O:28][C:29]1[CH:36]=[CH:35][C:32]([CH:33]=[CH2:34])=[CH:31][CH:30]=1)([CH3:27])([CH3:26])[CH3:25]>>[CH2:1]([O:3][CH:4]([O:6][C:7]1[CH:8]=[CH:9][C:10]([CH:11]=[CH2:12])=[CH:13][CH:14]=1)[CH3:5])[CH3:2].[OH:15][C:16]1[CH:23]=[CH:22][C:19]([CH:20]=[CH2:21])=[CH:18][CH:17]=1.[C:24]([O:28][C:29]1[CH:30]=[CH:31][C:32]([CH:33]=[CH2:34])=[CH:35][CH:36]=1)([CH3:27])([CH3:25])[CH3:26]

Komponenten

4

Versuchsvorschrift

To a solution of poly(p-hydroxystyrene/p-tert-butoxystyrene) (15.7 g) obtained in above (2) and ethyl vinyl ether (3.2 g) in 1,4-dioxane (140 ml), a catalytic amount of pyridinium p-toluenesulfonate was added and reacted with stirring at room temperature for 24 hours. The reaction mixture was poured into H2O (3 l) and the polymer was precipitated. The precipitate was filtered, washed with H2O and dried under reduced pressure to give 16.0 g of poly[p-(1-ethoxyethoxystyrene/p-hydroxystyrene/p-tert-butoxystyrene] as white powder having Mw 20000 (GPC with polystyrene calibration). The polymer was found to have p-(1-ethoxyethoxy)styrene unit, p-hydroxystyrene unit and p-tert-butoxystyrene unit in a molar ratio of ca. 30:60:10 based on 1HNMR.

Quellen und Nachweise

ORD-Eintrag
ord-e56fb72792424e79bb4caa6f82dba1bc
Quelldatensatz
uspto-grants-1996_09
Patentnummer
US05558976

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