Potassium hydride → Potassium (3-trimethylsiloxypropyl)-cyclopentadienide
Reaktionsgleichung
[H-].[K+:2].[CH3:3][Si:4]([CH3:15])([CH3:14])[O:5][CH2:6][CH2:7][CH2:8][C:9]1[CH2:13][CH:12]=[CH:11][CH:10]=1>O1CCCC1>[CH3:15][Si:4]([CH3:3])([CH3:14])[O:5][CH2:6][CH2:7][CH2:8][C-:9]1[CH:13]=[CH:12][CH:11]=[CH:10]1.[K+:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a suspension of 0.4 g (10 mmol) of potassium hydride in tetrahydrofurane, 1.96 g (10 mmol) of a (3-trimethylsiloxy-propyl)-cyclopentadiene in tetrahydrofurane is added. The reaction is maintained under stirring for 2 hours. Subsequently, the resulting suspension is concentrated to dryness, leaving an oily solid that, when it is washed with hexane, gives a cream-coloured solid. (1.6 g, 7 mmol. Yield:70%).
Aufarbeitung
- additionis added
- temperatureThe reaction is maintained
- concentrationSubsequently, the resulting suspension is concentrated to dryness
- customleaving an oily solid that, when it
- washis washed with hexane
- customgives a cream-coloured solid
Quellen und Nachweise
- ORD-Eintrag
- ord-21d514042e5546869747ebff7e22a158
- Quelldatensatz
- uspto-grants-2007_05
- Patentnummer
- US07211538B2
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