Trimethoxysilane → HCID 22486972, compound
Reaction equation
[CH:1]([CH:3]1[CH2:8][CH2:7][CH:6]([CH:9]=[CH2:10])[CH2:5][CH:4]1[CH:11]=[CH2:12])=[CH2:2].[CH3:13][O:14][SiH:15]([O:18][CH3:19])[O:16][CH3:17]>[Pt]>[CH3:13][O:14][Si:15]([O:18][CH3:19])([O:16][CH3:17])[CH2:2][CH2:1][CH:3]1[CH2:8][CH2:7][CH:6]([CH2:9][CH2:10][Si:15]([O:18][CH3:19])([O:16][CH3:17])[O:14][CH3:13])[CH2:5][CH:4]1[CH2:11][CH2:12][Si:15]([O:18][CH3:19])([O:16][CH3:17])[O:14][CH3:13]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
Into a 500 ml round-bottom flask, equipped with an addition funnel, thermometer, condenser and a magnetic stirrer, were charged 1,2,4-trivinylcyclohexane (50 grams, 0.31 mole, from Acros Organics) and platinum catalyst (10 ppm of H2PtCl6 solution from Sigma-Aldrich). The mixture was heated to 90° C. and dry air was bubbled into the reaction mixture. Trimethoxysilane (124 grams, 1.02 mole, from Momentive), was added to the flask using an addition funnel over a 70-minute period at such a rate as to maintain the reaction temperature at approximately 90° C. The reaction was recatalyzed with platinum catalysts (10 ppm of platinum-divinyltetramethyldisiloxane complex, containing 1.9% Pt, Karstedt's catalyst; see U.S. Pat. No. 377,452) and promoted with dried air sparge. The reaction was monitored using gas chromatography. After the reaction was complete, excess trimethoxysilane was removed by vacuum distillation. The final product is a clear yellow liquid.
Workup
- customInto a 500 ml round-bottom flask, equipped with an addition funnel
- customdry air
- customwas bubbled into the reaction mixture
- customover a 70-minute
- temperatureto maintain the reaction temperature at approximately 90° C
- customwith dried air
- customsparge
- customexcess trimethoxysilane was removed by vacuum distillation
Sources & evidence
- ORD record
- ord-9648f401cfa5401ca1d47e692910a8b7
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08809479B2
Reaction notes
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