Ethanol → HCID 86639774, compound
Reaction equation
[CH2:1]([O:3][Si:4]([C:11]12[CH2:17][CH:14]([CH2:15][CH2:16]1)[CH:13]=[CH:12]2)([O:8][CH2:9][CH3:10])[O:5][CH2:6][CH3:7])[CH3:2].C([SiH](CC)CC)C.C(O)C.[C:28]1(C)[CH:33]=CC=[CH:30][CH:29]=1>ClCCl.C1COCC1>[CH2:33]([C:11]12[CH2:17][CH:14]([CH2:15][CH2:16]1)[CH:13]=[CH:12]2)[CH2:28][CH2:29][CH3:30].[CH2:6]([O:5][Si:4]([C:11]12[CH2:17][CH:14]([CH2:15][CH2:16]1)[CH:13]=[CH:12]2)([O:8][CH2:9][CH3:10])[O:3][CH2:1][CH3:2])[CH3:7]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 80 °C
Procedure
BuNB (25.22 g, 0.168 mol), Triethoxysilyl Norbomene (TESNB, CAS 18401-43-9) (4.78 g, 0.019 mol), triethyl silane (0.11 g, 9.32E-05 mol), ethanol (0.10 g, 2.24E-03 mol) and toluene (170.0 g) were combined in a 500 mL serum bottle and heated to 80° C. in an oil bath to form a solution. To this solution were injected Pd1206 (0.018 g, 1.49E-05 mol) in the form of a concentrated solution in dichloromethane. After addition, the resulting mixture was maintained at 80° C. for 9 hours. The copolymer was precipitated by adding methanol drop wise into the vigorously stirred reaction mixture. The precipitated copolymer was collected by filtration and dried in an oven at 60° C. under vacuum After drying, 20.58 g was obtained (69%). The molecular weight of the copolymer was determined by GPC in THF solvent (polystyrene standard) to be Mw=238,000 and Mn=96,000. The composition of the copolymer was determined by 1H-NMR to be (85/15) BuNB/TESNB copolymer. The refractive indices of this polymer were measured by prism coupling method and determined to be 1.5061 in TE mode and 1.5041 in TM mode at a wavelength of 633 nm. The Tg (based on thermomechanical analysis (TMA) measurement) of this polymer was 276° C. The dried copolymer was dissolved insufficient toluene to result in a 30 wt % copolymer solution.
Workup
- customto form a solution
- additionAfter addition
- temperaturethe resulting mixture was maintained at 80° C. for 9 hours
- customThe copolymer was precipitated
- additionby adding methanol
- customdrop wise into the vigorously stirred reaction mixture
- filtrationThe precipitated copolymer was collected by filtration
- customdried in an oven at 60° C. under vacuum
- customAfter drying
- custom20.58 g was obtained (69%)
- customwas 276° C
- customto result in a 30 wt % copolymer solution
Sources & evidence
- ORD record
- ord-0093c3ab695842459bbdcbc7e34b1534
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07820356B2
Reaction notes
Loading…