HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17736Erstellt: 24. Oktober 2026
Ethyl Acetate → 4-(4-Chloro-3-ethylphenoxy)-1-nitrobenzene
https://huagongshe.com/de/reaction/17736
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | p-Fluoronitrobenzene | HCID 9590 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Chloro-3-ethylphenol | HCID 84223 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(4-Chloro-3-ethylphenoxy)-1-nitrobenzene | HCID 66977523 | — |
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-chloro-3-ethylphenol (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-(4-chloro-3-ethylphenoxy)-1-nitrobenzene. The crude product was used for further transformation.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07737285B2 |
|---|
| Quelldatensatz | uspto-grants-2010_06 |
|---|
| ORD ID | ord-c9b591b7bdb2490a88e07295fec5b175 |
|---|
| Quellennotiz | uspto-grants-2010_06 |
|---|