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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228825Generated: October 26, 2026

Hexane → (4,5-Dimethylfuran-2-yl)-(4-methyl-pyridin-2-yl)-methanol

https://huagongshe.com/reaction/228825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant4,5-Dimethyl-2-furaldehydeHCID 643406—
Reactant2-Bromo-4-methylpyridineHCID 2734087—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(4,5-Dimethylfuran-2-yl)-(4-methyl-pyridin-2-yl)-methanolHCID 2307847551.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-Bromo-4-picoline (1.5 g) was dissolved in tetrahydrofuran (40 ml) under an argon atmosphere to prepare a solution. A 1.6 M hexane solution (5.6 ml) of n-butyllithium was added dropwise to the solution at −78° C., and the mixture was then stirred at −78° C. for 30 min. A solution of 4,5-dimethylfurfural (1 g) in tetrahydrofuran (20 ml) was added dropwise thereto, and the temperature of the mixture was raised to room temperature with stirring. Water was added to the reaction solution to stop the reaction. The solvent was removed by distillation under the reduced pressure. Water was added to the residue, the mixture was extracted with ethyl acetate, and the ethyl acetate layer was then washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using hexane-ethyl acetate to give (4,5-dimethylfuran-2-yl)-(4-methyl-pyridin-2-yl)-methanol (904 mg, yield 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-81e12628fbb44c64921247d3f75181c9
Source noteuspto-grants-2009_07