Ethyl vinyl ether → p-1-Ethoxyethoxystyrene p-hydroxystyrene p-tetrahydropyranyloxystyrene
Reaction equation
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[CH2:7])=[CH:4][CH:3]=1.[O:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]1[O:16][C:17]1[CH:24]=[CH:23][C:20]([CH:21]=[CH2:22])=[CH:19][CH:18]=1.C(OC=C)C>>[CH2:11]([O:10][CH2:15][CH2:14][O:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[CH2:7])=[CH:4][CH:3]=1)[CH3:12].[OH:16][C:17]1[CH:24]=[CH:23][C:20]([CH:21]=[CH2:22])=[CH:19][CH:18]=1.[O:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]1[O:16][C:17]1[CH:18]=[CH:19][C:20]([CH:21]=[CH2:22])=[CH:23][CH:24]=1Participants
3
Procedure
Using 9.5 g of poly(p-hydroxystyrene/p-tetrahydropyranyloxystyrene) obtained according to (3) above and 2.7 g of ethylvinyl ether, reaction and after-treatments were carried out according to (3) of Preparation Example 3, and the produced crystals were filtered out, washed with water and dried in vacuo to give 9.9 g of poly(p-1-ethoxyethoxystyrene/p-hydroxystyrene/p-tetrahydropyranyloxystyrene) as white powdery crystal. P-1-ethoxyethoxystyrene unit/p-hydroxystyrene unit/p-tetrahydropyranyloxystyrene unit molar ratio in the polymer≈35:60:5 (1H NMR). Mw≈16,000; Mw/Mn=1.78 (GPC with polystyrene calibration).
Workup
- customobtained
- filtrationthe produced crystals were filtered out
- washwashed with water
- customdried in vacuo
Sources & evidence
- ORD record
- ord-be6daf759c5a44c089dd5cdbcefd24a0
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05976759
Reaction notes
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