反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=1.C1C[O:12][CH2:11][CH2:10]1.[Li+].CC([N-]C(C)C)C.C1OC1>O>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][CH2:10][CH2:11][OH:12])[N:3]=1参加物
6
反応条件
- 温度
- -78 °C
実験手順
To a solution of 2-fluoro-6-methylpyridin (27 mmol) in 65 ml of freshly distilled THF was added via syringe 13.5 ml of 2M LDA, and the resulting mixture was stirred at -78° C. for 20 min. To the above cold solution was added 4 ml of 4M ethylene oxide and the mixture was allowed to warm to room temperature which stirring. The mixture was diluted with water, extracted with ether, and the organic layer was washed with water (2×) and brine, and dried over sodium sulfate. The organic solution was concentrated, and the residue was purified by flash chromatography (chloroform/ethanol, 10:1) to yield 1.3 g (30.9%) of 2-fluoro-6-(3-hydroxypropyl)pyridine, as a yellow oil.
後処理
- temperatureto warm to room temperature which
- stirringstirring
- extractionextracted with ether
- washthe organic layer was washed with water (2×) and brine
- dry with materialdried over sodium sulfate
- concentrationThe organic solution was concentrated
- customthe residue was purified by flash chromatography (chloroform/ethanol, 10:1)
出典と根拠
- ORDレコード
- ord-a40c09c9f82c43a7b1fa57d35d1dc6a0
- 出典データセット
- uspto-grants-1998_06
- 特許番号
- US05763461
関連ノート
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