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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 332569Erstellt: 26. Oktober 2026

Hydrochloric Acid → 1-Fluoro-2-(4-fluoro-phenoxy)-3-Methoxy benzene

https://huagongshe.com/reaction/332569

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktN,N-DimethylglycineHCID 673—
Edukt4-FluoroiodobenzeneHCID 9605—
EduktCesium carbonateHCID 10796—
Edukt2-Fluoro-6-methoxyphenolHCID 2737367—
KatalysatorCopperHCID 23978—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-Fluoro-2-(4-fluoro-phenoxy)-3-Methoxy benzeneHCID 577011186.350,2%

Reaktionsbedingungen

Temperatur105 °C

Reaktionsschritte

To a suspension of 2-fluoro-6-methoxy phenol (1) (2.8 g, 20 mmol), N,N-dimethyl glycine.HCl (837 mg, 6 mmol), Cs2CO3 (13 g, 40 mmol), 1-fluoro-4-iodobenzene (2.3 mL, 20 mmol), in Dioxane (40 ml) was added copper iodone (381 mg, 2 mmol). The reaction mixture was stirred at 105° C. over 1 week. Upon heating the reaction mixture turned from brown to a bright green. After cooling to room temperature, the reaction mixture was filtered and the filtrate was concentrated in-vacuo. The crude was purified by silica gel eluted with hexane/EtOAc (10:1), concentrated in-vacuo, to provide 300 g (21% yield) of product (2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08877816B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-6114c9b5157c4a06afa58a4a0bff2316
Quellennotizuspto-grants-2014_11