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

HRID 743926

Reaktionsgleichung

Reaktionsgleichung von HRID 743926
[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-ethoxyethoxy-styrene/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-tertbutoxystyrene unit in a molar ratio of ca. 30:60:10 based on 1HNMR.

Quellen und Nachweise

ORD-Eintrag
ord-3d0652d8a03b4e2890f99f84aefd931c
Quelldatensatz
uspto-grants-1996_09
Patentnummer
US05558971

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