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HRID 229048作成日:2026年10月26日

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

https://huagongshe.com/reaction/229048

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-Bromo-3-methylpyridineHCID 220832—
反応物4,5-Dimethyl-2-furaldehydeHCID 643406—
反応物HCID 178418244HCID 178418244—
溶媒TetrahydrofuranHCID 8028—
生成物(4,5-Dimethylfuran-2-yl)-(3-methylpyridin-2-yl)-methanolHCID 2307846566.8%

反応条件

温度-78 °C

反応手順

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%).

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-f0baf40a238143caa1fab31eebd1a521
出典メモuspto-grants-2009_07