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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376277Generated: October 30, 2026

Furan → 2-(2-Furanyl)-6-methylpyridine

https://huagongshe.com/reaction/376277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuranHCID 8029—
ReactantHCID 10847672HCID 10847672—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-(2-Furanyl)-6-methylpyridineHCID 1936174581.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

40 ml of a 1.6 M solution of n-butyllithium in hexane are introduced dropwise into a solution of 4.36 ml of furan (60 mmol) and 40 ml of tetrahydrofuran cooled to 0° C. The solution is stirred for 3 hours at 0° C. and then it is cooled to -40° C. before introducing 120 ml of a 0.5 M solution of zinc dichloride in tetrahydrofuran. The mixture is stirred for 2 hours at room temperature and then the reaction mixture is added to a solution of 9.17 g of trifluoromethanesulfonic acid 6-methylpyridin-2-yl ester (40 mmol) in 20 ml of tetrahydrofuran containing 2.30 g of tetrakis-(triphenylphosphine)palladium (2 mmol). The reaction mixture is maintained under reflux for 2 hours under nitrogen and then cooled and extracted with 1N HCl. The acidic aqueous phase is neutralized with 10N NaOH and then extracted with ethyl acetate. The organic phase is washed with water, dried over magnesium sulfate, filtered and the solvent evaporated off. The expected product is isolated by rectification under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020345
Source datasetuspto-grants-2000_02
ORD IDord-93fc0c56b937438a86878fc53e39b615
Source noteuspto-grants-2000_02