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HRID 228795생성일: 2026년 10월 23일

Hexane → (4,5-Dimethylfuran-2-yl)-(4,5-dimethylthiazol-2-yl)methanol

https://huagongshe.com/ko/reaction/228795

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물4,5-DimethylthiazoleHCID 62510—
반응물4,5-Dimethyl-2-furaldehydeHCID 643406—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(4,5-Dimethylfuran-2-yl)-(4,5-dimethylthiazol-2-yl)methanolHCID 2307835450%

반응 조건

온도-78 °C

반응 단계

4,5-Dimethylthiazole (1.0 g) was dissolved in tetrahydrofuran (40 ml) under an argon atmosphere to prepare a solution. A 1.6M hexane solution (5.6 ml) of n-butyllithium was added dropwise 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 with 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-acetone to give (4,5-dimethylfuran-2-yl)-(4,5-dimethylthiazol-2-yl)methanol (945 mg, yield 50%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-180cca5b01ff4d8e8ae7e372138e4049
출처 메모uspto-grants-2009_07