HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1753708Erstellt: 25. Oktober 2026
Ethanol → 3,7-Bis(5-methoxybiphenyl-2-yl)dibenzo[b,d]thiophene
https://huagongshe.com/reaction/1753708
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 3,7-Dibromodibenzo(b,d)thiophene | HCID 803759 | — |
| Edukt | (4-Methoxy-2-phenylphenyl)boronic acid | HCID 85664000 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 3,7-Bis(5-methoxybiphenyl-2-yl)dibenzo[b,d]thiophene | HCID 86730006 | 81% |
Reaktionsschritte
A mixture of 3.42 g (10 mmol) of 3,7-dibromodibenzo[b,d]thiophene, 5.5 g (24 mmol) of 5-methoxybiphenyl-2-ylboronic acid, 0.12 g (0.1 mmol) of tetrakis(triphenylphosphine)palladium, 15 ml of 2M Na2CO3, 20 ml of EtOH and 60 ml toluene was degassed and placed under nitrogen, then heated at 110° C. for 8 h. After finishing the reaction, the mixture was allowed to cool to room temperature. The reaction mixture was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was evaporated in vacuum. The residue was purified by column chromatography on silica(hexane-dichloromethane) to afford a white solid (4.4 g, 8.1 mmol, 81%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09166177B2 |
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| Quelldatensatz | uspto-grants-2015_10 |
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| ORD ID | ord-6ee38b1af7ef4ae69d88d9cf2818fa87 |
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| Quellennotiz | uspto-grants-2015_10 |
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