Methyl Methacrylate → HCID 86750009, compound
Reaction equation
[C:1]([O:6][CH3:7])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:8]([O:13][CH2:14][CH:15]1[O:17][CH2:16]1)(=[O:12])[C:9]([CH3:11])=[CH2:10].[C:18]([O:23][CH2:24][CH2:25][OH:26])(=[O:22])[C:19]([CH3:21])=[CH2:20]>>[C:1]([O:6][CH3:7])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:8]([O:13][CH2:14][CH:15]1[O:17][CH2:16]1)(=[O:12])[C:9]([CH3:11])=[CH2:10].[C:18]([O:23][CH2:24][CH2:25][OH:26])(=[O:22])[C:19]([CH3:21])=[CH2:20]Participants
4
Procedure
Using methyl methacrylate (35.0 g, 0.35 mole), glycidyl methacrylate (28.4 g, 0.2 mole) and 2-hydroxyethyl methacrylate (13.0 g, 0.1 mole), the polymerization was carried out in the same manner as described in Synthesis Example 12, (1), and the precipitate was filtered and dried under reduced pressure to give 70.3 g of poly(methyl methacrylate/glycidyl methacrylate/2-hydroxyethyl methacrylate) as white powders having Mw 35000 and Mn 192000 (GPC with polystyrene calibration).
Workup
- customas described in Synthesis Example 12, (1),
- filtrationthe precipitate was filtered
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-0c38098e70da417daa88354498885fb0
- Source dataset
- uspto-grants-1997_10
- Patent number
- US05677112
Reaction notes
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