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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229048Generated: October 26, 2026

Water → (4,5-Dimethylfuran-2-yl)-(3-methylpyridin-2-yl)-methanol

https://huagongshe.com/reaction/229048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Bromo-3-methylpyridineHCID 220832—
Reactant4,5-Dimethyl-2-furaldehydeHCID 643406—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product(4,5-Dimethylfuran-2-yl)-(3-methylpyridin-2-yl)-methanolHCID 2307846566.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-Bromo-3-methylpyridine (1.53 g) was dissolved in tetrahydrofuran (40 ml) under an argon atmosphere to prepare a solution. A 1.6M n-butyllithium/n-hexane solution (5.7 ml) 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 (1.00 g) in tetrahydrofuran (20 ml) was added dropwise thereto, and the temperature of the mixture was raised to room temperature while 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, and the mixture was extracted with ethyl acetate. 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)-(3-methyl-pyridin-2-yl)-methanol (1.17 g, yield 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-f0baf40a238143caa1fab31eebd1a521
Source noteuspto-grants-2009_07