2-Hydroxypropyl methacrylate → Ibma hpma
Reaction equation
[CH3:1][C:2]([C:4]([O:6][CH:7]1[C@@:12]2([CH3:16])[C:13]([CH3:15])([CH3:14])[C@H:9]([CH2:10][CH2:11]2)[CH2:8]1)=[O:5])=[CH2:3].[CH3:17][CH:18]([OH:26])[CH2:19][O:20][C:21]([C:23]([CH3:25])=[CH2:24])=[O:22]>>[CH3:3][C:2]([C:4]([O:6][CH:7]1[C@@:12]2([CH3:16])[C:13]([CH3:15])([CH3:14])[C@H:9]([CH2:10][CH2:11]2)[CH2:8]1)=[O:5])=[CH2:1].[CH3:17][CH:18]([OH:26])[CH2:19][O:20][C:21]([C:23]([CH3:25])=[CH2:24])=[O:22]Participants
3
Procedure
CHMA, BMA, IBMA and HPMA residues were copolymerized using a halogenated CPO initiator according to the following:
Workup
- customcopolymerized
Sources & evidence
- ORD record
- ord-6c6820c627b949c0b498e83dbd366a4e
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06576722B2
Reaction notes
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