Acetone → Stearyl glycidyl ether octyl glycidyl ether
Reaction equation
[CH2:1]([O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])[CH:2]1[O:4][CH2:3]1.[C:14]1([CH3:20])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.Cl.[CH3:22][C:23]([CH3:25])=O>>[CH2:1]([O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:22][CH2:23][CH2:25][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:14][CH3:20])[CH:2]1[O:4][CH2:3]1.[CH2:1]([O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])[CH:2]1[O:4][CH2:3]1Participants
5
Procedure
50 mL of Catalyst B, 40.0 g of stearyl glycidyl ether (SGE) and 22.8 g of octyl glycidyl ether (OGE) were added to 210 ml of toluene, and a vessel was closed. The polymerization was carried out at 130° C. for 24 hours with stirring. The reaction solution was added to a large amount of acetone containing a small amount of a dilute solution of hydrogen chloride. A precipitated solid was dried under reduced pressure at 80° C. for 24 hours to obtain a poly(stearyl glycidyl ether/octyl glycidyl ether) copolymer. Pale yellow solid. Yield 75%.
Workup
- customwas closed
- customA precipitated solid was dried under reduced pressure at 80° C. for 24 hours
Sources & evidence
- ORD record
- ord-9909a9a5f8c54061893a864b5514024b
- Source dataset
- uspto-grants-2004_10
- Patent number
- US06800723B2
Reaction notes
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