Trichlorooctadecylsilane → 12-[2-[2-(2-Methoxyethoxy)ethoxy]ethoxy]-12-octadecyl-2,5,8,11,13,16,19,22-octaoxa-12-silatricosane
Reaction equation
[CH2:1]([Si:19](Cl)(Cl)Cl)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[CH3:23][O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29][O:30][CH2:31][CH2:32][OH:33]>CCCCCCC>[CH2:1]([Si:19]([O:33][CH2:32][CH2:31][O:30][CH2:29][CH2:28][O:27][CH2:26][CH2:25][O:24][CH3:23])([O:33][CH2:32][CH2:31][O:30][CH2:29][CH2:28][O:27][CH2:26][CH2:25][O:24][CH3:23])[O:33][CH2:32][CH2:31][O:30][CH2:29][CH2:28][O:27][CH2:26][CH2:25][O:24][CH3:23])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]Participants
4
Procedure
The procedure of Example 1 was repeated with 387.5 g (1.0 mole) of octadecyltrichlorosilane and 800 mL of heptane. Under nitrogen 508.4 g (3.10 mole) of 2-(2-(2-methoxyethoxy)ethoxy)ethanol was added at 80° C. over 4 hours. After heating the reaction for an additional 48 hours and removal of all volatile components under vacuum, 780 g of the pale yellow liquid product were obtained.
Workup
- temperatureAfter heating
- customthe reaction for an additional 48 hours
- customremoval of all volatile components under vacuum
Sources & evidence
- ORD record
- ord-fdac2874a1f24ac4b7ad8403a80d9772
- Source dataset
- uspto-grants-1996_09
- Patent number
- US05552476
Reaction notes
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