1-(1-Methyl-1H-imidazol-2-yl)ethan-1-one → 2-(1-methyl-1H-imidazol-2-yl)but-3-yn-2-ol
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Br[Mg][C:3]#[CH:4].[CH3:5][N:6]1[CH:10]=[CH:9][N:8]=[C:7]1[C:11](=[O:13])[CH3:12]>O1CCCC1>[CH3:5][N:6]1[CH:10]=[CH:9][N:8]=[C:7]1[C:11]([OH:13])([C:3]#[CH:4])[CH3:12]참가 물질
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- 온도
- 0 °C
실험 절차
Into a 250-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed bromo(ethynyl)magnesium (0.5M in THF, 77 mL, 1.20 equiv). This was followed by the addition of a solution of 1-(1-methyl-1H-imidazol-2-yl)ethan-1-one (4.0 g, 32.22 mmol, 1.00 equiv) in tetrahydrofuran (15 mL) dropwise with stirring at 0° C. in 20 min. The resulting solution was stirred for 20 min at 0° C. The resulting solution was allowed to react with stirring for an additional 5 h at room temperature. The reaction was then quenched by the addition of 50 mL of saturated aqueous NH4Cl. The resulting solution was extracted with 3×100 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/hexane (1/3) to give 2.8 g (58%) of 2-(1-methyl-1H-imidazol-2-yl)but-3-yn-2-ol as a off-white solid. 1H-NMR (300 MHz, CDCl3, ppm) δ 7.065 (d, 1H), 6.842 (d, 1H), 3.935 (d, 3H), 3.092 (s, 3H), 1.950 (s, 3H).
후처리
- customInto a 250-mL 3-necked round-bottom flask purged
- temperaturemaintained with an inert atmosphere of nitrogen
- stirringThe resulting solution was stirred for 20 min at 0° C
- customto react
- stirringwith stirring for an additional 5 h at room temperature
- customThe reaction was then quenched by the addition of 50 mL of saturated aqueous NH4Cl
- extractionThe resulting solution was extracted with 3×100 mL of ethyl acetate
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated under vacuum
출처 및 근거
- ORD 기록
- ord-7c11520656b24df38e12cb73cd5c033d
- 출처 데이터셋
- uspto-grants-2015_05
- 특허 번호
- US09034866B2
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