Vinyltrimethoxysilane → HCID 131728817, compound
Reaction equation
[CH:1]([Si:3](OC)([O:6][CH3:7])[O:4][CH3:5])=[CH2:2].[CH:10]([Mg]Br)([CH3:12])[CH3:11].C[O-].[Mg+2].C[O-]>C(OCC)C>[CH:10]([CH:2]=[CH:1][SiH:3]([O:6][CH3:7])[O:4][CH3:5])([CH3:12])[CH3:11]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
206 g (1.39 mol) of vinyl trimethoxysilane and 300 ml of dry diethyl ether were charged in a 2 L four-necked flask equipped with a dropping funnel and a mechanical stirrer in a stream of nitrogen, and cooled to 0° C. 1.67 mol of the above prepared diethyl ether solution of isopropyl magnesium bromide was dropwise added thereto with stirring over a period of 120 minutes, and reaction was carried out at room temperature for 2 hours. After completion of the reaction, magnesium methoxide residue as a by-product was removed by filtration, and the obtained filtrate was distilled under reduced pressure to obtain 141 g (0.882 mol) of isopropylvinyldimethoxysilane as an aimed product. The yield was 63.5%.
Workup
- customequipped with a dropping funnel and a mechanical stirrer in a stream of nitrogen
- additionwas dropwise added
- customreaction
- waitwas carried out at room temperature for 2 hours
- customwas removed by filtration
- distillationthe obtained filtrate was distilled under reduced pressure
Sources & evidence
- ORD record
- ord-c186988e378841c5835410c5e83c5e13
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07935425B2
Reaction notes
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