HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17729Erstellt: 26. Oktober 2026
4-Hydroxybiphenyl → 4-(4-Nitrophenoxy)-1,1'-biphenyl
https://huagongshe.com/reaction/17729
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Hydroxybiphenyl | HCID 7103 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | p-Fluoronitrobenzene | HCID 9590 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(4-Nitrophenoxy)-1,1'-biphenyl | HCID 240864 | — |
Reaktionsschritte
To a stirred solution of 1-fluoro-4-nitrobenzene (10 mmol) in DMF (20 mL) at room temperature, solid K2CO3 (30 mmol) was added followed by addition of 4-hydroxybiphenyl (10 mmol) to the reaction mixture and heating to 80° C. until the reaction was complete as indicated by TLC or HPLC. After cooling to room temperature to room temperature, the reaction mixture was poured into EtOAc (100 mL), washed with water (2×50 mL) and brine (50 mL), and dried over sodium sulfate. The solvent was removed in vacuo to afford the desired 4-(biphenyl-4-oxy)-1-nitrobenzene. The crude product was used for further transformation.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737285B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-1bf6e80c0a96446baa085c6ab281ef86 |
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| Quellennotiz | uspto-grants-2010_06 |
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