Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chlorotrimethylgermane | HCID 73723 | — |
| Edukt | 6-Bromo-2-(3,5-dimethylphenyl)quinoline | HCID 68193681 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 86669968 | HCID 86669968 | — |
Reaktionsschritte
6-Bromo-2-(3,5-dimethylphenyl)quinoline (6.0 g, 19.2 mmol) and 150 mL anhydrous THF were added in a dry 2-necked round bottom flask and cooled down to −78° C. 8.46 mL BuLi (2.5 M in hexane) was added dropwise. The solution was stirred for 45 minutes at −78° C. and 2.83 mL (23.06 mmol) of chlorotrimethylgermane was slowly added with a syringe. The solution was stirred for overnight. The reaction mixture was purified by column 5% ethyl acetate in hexane and distillation. ˜4.1 g white slide was obtained after recrystallization from hexane. GC-MS confirmed the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08492006B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-d8535ac3f80b4ef29b8ad6cf130827e7 |
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| Quellennotiz | uspto-grants-2013_07 |
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