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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Eduktp-FluoronitrobenzeneHCID 9590—
EduktPotassium CarbonateHCID 11430—
Edukt4-Chloro-3-ethylphenolHCID 84223—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(4-Chloro-3-ethylphenoxy)-1-nitrobenzeneHCID 66977523—

Reaktionsbedingungen

Temperatur80 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737285B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-c9b591b7bdb2490a88e07295fec5b175
Quellennotizuspto-grants-2010_06