Reaktionsgleichung
[CH3:1][C:2]1[CH2:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].Cl[CH2:10][CH2:11][CH2:12][Si:13]([O:17][CH3:18])([O:15][CH3:16])[CH3:14]>C(OCC)C>[CH3:1][C:2]1[CH:6]=[CH:5][CH:4]([CH2:10][CH2:11][CH2:12][Si:13]([O:17][CH3:18])([O:15][CH3:16])[CH3:14])[CH:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
33.4 g (417 mmol) of freshly distilled methylcyclopentadiene are added dropwise to a suspension of 10 g (417 mmol) of sodium hydride in 250 ml of absolute diethyl ether at RT over a period of one hour. 76.1 g of (3-chloropropyl)dimethoxy-methylsilane are subsequently added dropwise over a period of 30 minutes. The solution becomes warm during this process. After taking off the solvent, the mixture is fractionally distilled in an oil pump vacuum to give 78.9 g of (3-methylcyclopentadienylpropyl)dimethoxy-methylsilane (yield: 89%).
Aufarbeitung
- temperatureThe solution becomes warm during this process
- distillationthe mixture is fractionally distilled in an oil pump vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-e7f0e7d29f5b4d428bc0d19bf8ae4bf4
- Quelldatensatz
- uspto-grants-2012_01
- Patentnummer
- US08088878B2
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