Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | p-Fluoronitrobenzene | HCID 9590 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Dibenzofuranol | HCID 66587 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(Dibenzofuran-2-yloxy)-1-nitrobenzene | HCID 2102893 | — |
Reaktionsschritte
To a stirred solution of 1-fluoro-4-nitrobenzene (10 mmol) in DMF (20 mL) at rt, solid potassium carbonate (30 mmol) was added followed by addition of 2-hydroxydibenzofuran (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 rt, the reaction mixture was poured into H2O (100 mL), extracted with EtOAc (2×50 mL), washed with H2O (2×50 mL) and brine (50 mL), and dried over sodium sulfate. The solvent was removed in vacuuo to afford the desired 4-(dibenzofuran-2-yloxy)-1-nitrobenzene. The crude product was used for further transformation.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07361678B2 |
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| Quelldatensatz | uspto-grants-2008_04 |
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| ORD ID | ord-b37056e339894a4e902d243f326f8560 |
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| Quellennotiz | uspto-grants-2008_04 |
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