HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17725Erstellt: 25. Oktober 2026
Ethyl Acetate → 4-(4-Chloro-2-cyclohexylphenoxy)-1-nitrobenzene
https://huagongshe.com/reaction/17725
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | p-Fluoronitrobenzene | HCID 9590 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Chloro-2-cyclohexylphenol | HCID 83120 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(4-Chloro-2-cyclohexylphenoxy)-1-nitrobenzene | HCID 66977404 | — |
Reaktionsschritte
To a stirred solution of 1-fluoro-4-nitrobenzene (10 mmol) in DMF (10 mL) at rt, solid potassium carbonate (30 mmol) was added followed by addition of 4-chloro-2-cyclohexylphenol (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 (80 ml), washed with H2O (2×40 ml) and brine (60 mL), and dried over sodium sulfate. The solvent was removed in vacuuo to afford the desired 4-(4-chloro-2-cyclohexylphenoxy)-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-31e3056647044bc28e7ac833a0dea674 |
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| Quellennotiz | uspto-grants-2010_06 |
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