돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 229048생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/229048

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Bromo-3-methylpyridineHCID 220832—
반응물4,5-Dimethyl-2-furaldehydeHCID 643406—
반응물HCID 178418244HCID 178418244—
용매TetrahydrofuranHCID 8028—
생성물(4,5-Dimethylfuran-2-yl)-(3-methylpyridin-2-yl)-methanolHCID 2307846566.8%

반응 조건

온도-78 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-f0baf40a238143caa1fab31eebd1a521
출처 메모uspto-grants-2009_07