HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270735Erstellt: 24. Oktober 2026
1,1',1''-(Chlorosilylidyne)tris(benzene) → 9-Bromo-l0-triphenysilyl anthracene
https://huagongshe.com/de/reaction/270735
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,1',1''-(Chlorosilylidyne)tris(benzene) | HCID 6458 | — |
| Edukt | 9,10-Dibromoanthracene | HCID 68226 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 9-Bromo-l0-triphenysilyl anthracene | HCID 59833959 | — |
Reaktionsschritte
In a nitrogen atmosphere, 12 g (35.7 mmol) of 9,10-dibromoanthracene, and 300 ml of tetrahydrofuran (THF) were added to a round-bottom flask. Next, 14.4 ml (35.7 mmol, 2.5M) of n-butyl lithium was added dropwise slowly into the round-bottom flask at −78° C. After mixing and reacting for 30 min, 12 g (40.7 mmol) triphenylsilyl chloride with 50 ml THF were added dropwise slowly into the round-bottom flask at −78° C. After reacting at room temperature for 24 hours, the resulting mixture was subjected to extraction with a mixed solvent (ethyl acetate:H2O), dried over anhydrous MgSO4, filtered, and condensed, then the crude product was purified by column chromatography (n-hexane/acetyl acetate=15/1), A 9.0 g of pure 9-bromo-10-triphenysilyl anthracene was collected.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07449593B2 |
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| Quelldatensatz | uspto-grants-2008_11 |
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| ORD ID | ord-fecb7ac6bffa4b2094f2007780da8def |
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| Quellennotiz | uspto-grants-2008_11 |
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