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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228817Generated: October 26, 2026

Hexane → (4,5-Dimethylfuran-2-yl)-(6-methyl-pyridin-2-yl)-methanol

https://huagongshe.com/reaction/228817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant2-Bromo-6-methylpyridineHCID 79205—
Reactant4,5-Dimethyl-2-furaldehydeHCID 643406—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(4,5-Dimethylfuran-2-yl)-(6-methyl-pyridin-2-yl)-methanolHCID 2307835380%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-Bromo-6-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 while stirring. Water was added to the reaction solution to stop the reaction, and 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-acetone to give (4,5-dimethylfuran-2-yl)-(6-methyl-pyridin-2-yl)-methanol (1.4 g, yield 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-184fa0e40e7b4fb6846e0d92c287f54f
Source noteuspto-grants-2009_07