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HRID 228817作成日:2026年10月27日

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

https://huagongshe.com/reaction/228817

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物2-Bromo-6-methylpyridineHCID 79205—
反応物4,5-Dimethyl-2-furaldehydeHCID 643406—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(4,5-Dimethylfuran-2-yl)-(6-methyl-pyridin-2-yl)-methanolHCID 2307835380%

反応条件

温度-78 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560558B2
出典データセットuspto-grants-2009_07
ORD IDord-184fa0e40e7b4fb6846e0d92c287f54f
出典メモuspto-grants-2009_07