Reaktionsgleichung
C[Si]([Cl:5])(C)C.[OH-].[CH:7]1([Sn+:13]([CH:20]2[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)[CH:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1>>[CH:20]1([Sn:13]([Cl:5])([CH:7]2[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12]2)[CH:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]1Komponenten
3
Versuchsvorschrift
In a 500 mL three-necked flask, trimethylsilyl chloride (170 g, 109 mmol) was added to tricyclohexyltin hydroxide (80 g, 133 mmol) and heated at reflux during 18 hours. After distillation of trimethylsilyl chloride in excess and hexamethyldisiloxane under reduced pressure, the crude product was recrystallized in petroleum ether. White needles were obtained (39.82 g, 79.6 mmol).
Aufarbeitung
- temperatureheated
- temperatureat reflux during 18 hours
- distillationAfter distillation of trimethylsilyl chloride in excess and hexamethyldisiloxane under reduced pressure
- customthe crude product was recrystallized in petroleum ether
- customWhite needles were obtained (39.82 g, 79.6 mmol)
Quellen und Nachweise
- ORD-Eintrag
- ord-188e8eb6b60a451ca46c1ccd7ff9703f
- Quelldatensatz
- uspto-grants-2010_03
- Patentnummer
- US07687581B2
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