HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17734Erstellt: 25. Oktober 2026
Ethyl Acetate → 1-(4-Fluorophenoxy)-2-nitrobenzene
https://huagongshe.com/reaction/17734
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | p-Fluoronitrobenzene | HCID 9590 | — |
| Edukt | 4-Fluorophenol | HCID 9732 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-(4-Fluorophenoxy)-2-nitrobenzene | HCID 961127 | — |
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 4-fluorophenol (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 EtOAc (100 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-fluorophenoxy-1-nitrobenzene. The crude product may be used for further transformation.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07737285B2 |
|---|
| Quelldatensatz | uspto-grants-2010_06 |
|---|
| ORD ID | ord-b7e95b37aff74c7da58bf91ff97b660b |
|---|
| Quellennotiz | uspto-grants-2010_06 |
|---|