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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3076Erstellt: 23. Oktober 2026

1-Bromo-2,4-difluorobenzene → 3(2,4-Difluorophenyl)thiophene

https://huagongshe.com/de/reaction/3076

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-2,4-difluorobenzeneHCID 67674—
Edukt1-Bromo-3,4,5-trifluorobenzeneHCID 611409—
Edukt3-(3,4,5-Trifluorophenyl)thiopheneHCID 23295528—
Produkt3(2,4-Difluorophenyl)thiopheneHCID 2274369297%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

The same procedures set forth above in Example (1)(a) for synthesizing 3(3,4,5-trifluorophenyl)thiophene were followed, with the exception that 1-bromo-2,4-difluorobenzene was substituted for 1-bromo-3,4,5-trifluorobenzene as the 1-bromo-substituted fluorobenzene, and the coupling reaction mixture was heated to reflux in an oil bath for 10 hours with stirring at 80° C. (as opposed to being heated in an oil bath for 0.5 hour with periodically stirring). No further purification by recrystallization was required to obtain a 97 to 98% pure product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05733683
Quelldatensatzuspto-grants-1998_03
ORD IDord-84962d33083243bb8070accd1465b529
Quellennotizuspto-grants-1998_03