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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550023Generated: October 26, 2026

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

https://huagongshe.com/reaction/550023

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-BithiopheneHCID 68120—
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(5-Fluoro-2-thienyl)thiopheneHCID 6660840371.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943788B2
Source datasetuspto-grants-2011_05
ORD IDord-19ec49aac26848e29fa5795c439a7856
Source noteuspto-grants-2011_05