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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 221130Erstellt: 25. Oktober 2026

2,2'-Bithiophene → 2-(5-Fluoro-2-thienyl)thiophene

https://huagongshe.com/reaction/221130

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,2'-BithiopheneHCID 68120—
EduktN-FluorobenzenesulfonimideHCID 588007—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(5-Fluoro-2-thienyl)thiopheneHCID 6660840371,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

2,2′-Bithiophene (7.40 g) in tetrahydrofuran (90 ml) was cooled to −78° C. under argon atmosphere, and thereto were added dropwise n-butyl lithium (1.59 M hexane solution, 28.0 ml). The mixture was stirred at 0° C. for one 30 minutes, and cooled again to −78° C. Added thereto was N-fluorobenzenesulfonimide (15.5 g), and the mixture was gradually warmed, and stirred at room temperature for 17 hours. The reaction mixture was poured into ice-cold water, and the solution was extracted with hexane twice, and the extract was washed successively with water and brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (hexane) to give 2-(5-fluoro-2-thienyl)thiophene (5.89 g) as colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202984B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-7f440e9e3b7342a2ad87bdf0a40e9c57
Quellennotizuspto-grants-2012_06