HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Toluene → 1,2-Bisfluorenyltetramethyldisilane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | 1,2-Dichloro-1,1,2,2-tetramethyldisilane | HCID 78045 | — |
| Edukt | 2,7-Dibromo-9,9-di-n-octylfluorene | HCID 5215321 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1,2-Bisfluorenyltetramethyldisilane | HCID 21889333 | — |
Reaktionsschritte
Under a nitrogen gas atmosphere, 4.99 g (9.10 mmol) of 2,7-dibromo-9,9-dioctylfluorene, 20 ml of diethyl ether and 10 ml of toluene were added to a 100 ml three-necked flask equipped with a reflux condenser and a dropping funnel. Under cooling by an ice bath, 6.2 ml (9.92 mmol) of a hexane solution of n-butyllithium (1.6 M) was added dropwise. As the butyllithium was added dropwise, the solution turned red. This solution was agitated “as is” for approximately 1 hour; then, 810 mg (4.33 mmol) of 1,2-dichlorotetramethyldisilane was added, and the resulting mixture was agitated and reacted all night.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07135242B2 |
| Quelldatensatz | uspto-grants-2006_11 |
| ORD ID | ord-213509883d0a4b648c0eeb2ca8191239 |
| Quellennotiz | uspto-grants-2006_11 |