Trimethoxysilane → HCID 53673316, compound
Reaction equation
[C:1]([O:7][CH2:8][CH:9]=[CH2:10])(=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5].[CH3:11][O:12][SiH:13]([O:16][CH3:17])[O:14][CH3:15]>[Pt]>[C:1]([O:7][CH2:8][CH2:9][CH2:10][Si:13]([O:16][CH3:17])([O:14][CH3:15])[O:12][CH3:11])(=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirrer bar was put into a 50 ml two-mouth eggplant flask equipped with a thermometer and a calcium chloride tube. The flask was charged with 5.13 g (40 mmol) of allyl valerate (manufactured by Aldrich Co.) and 0.2 g of a platinum catalyst (“BY 24-835” manufactured by a Toray-Dow Corning Co.). Then, 4.89 g (40 mmol) of trimethoxysilane (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was added while stirring and controlling the temperature at 50° C. or less. After further addition of 0.2 g of the platinum catalyst, the mixture was reacted at room temperature for six hours. After completion of the reaction, the reaction mixture was distilled under reduced pressure using a Kugelrohr distillation apparatus to obtain 8.12 g of 3-trimethoxysilylpropyl valerate of the silane compound (1).
Workup
- customequipped with a thermometer and a calcium chloride tube
- customat 50° C. or less
- customthe mixture was reacted at room temperature for six hours
- customAfter completion of the reaction
- distillationthe reaction mixture was distilled under reduced pressure
- distillationa Kugelrohr distillation apparatus
Sources & evidence
- ORD record
- ord-331c0edc550a465f9d21467046e0bc05
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08481669B2
Reaction notes
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