反応式
II.Br[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH3:12])=[CH:6][CH:5]=1.[Mg].[CH:14]1([C:17]2[CH:18]=[CH:19][C:20]([CH:25]=[O:26])=[N:21][C:22]=2[O:23][CH3:24])[CH2:16][CH2:15]1>C1COCC1>[CH:14]1([C:17]2[CH:18]=[CH:19][C:20]([CH:25]([C:4]3[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH3:12])=[CH:6][CH:5]=3)[OH:26])=[N:21][C:22]=2[O:23][CH3:24])[CH2:16][CH2:15]1参加物
反応条件
- 温度
- 50 °C
実験手順
A small amount of iodine was added to a suspension of 1-bromo-4-ethoxybenzene (484 μL) and magnesium (82.3 mg) in THF at room temperature in a nitrogen atmosphere, and the mixture was stirred at 50° C. for one hour. The reaction solution was returned to room temperature and a solution of 5-cyclopropyl-6-methoxypyridine-2-carbaldehyde (300 mg) in tetrahydrofuran (1 mL) was added, followed by stirring at 50° C. for one hour. Tetrahydrofuran was concentrated under reduced pressure and a saturated ammonium chloride solution was added, followed by extraction with ethyl acetate. The organic layer was filtered through diatomaceous earth, and then the solvent was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=50:1→9:1) to give (5-cyclopropyl-6-methoxypyridin-2-yl)(4-ethoxyphenyl)methanol as a yellow oil (438 mg, 86%).
後処理
- customwas returned to room temperature
- stirringby stirring at 50° C. for one hour
- concentrationTetrahydrofuran was concentrated under reduced pressure
- additiona saturated ammonium chloride solution was added
- extractionfollowed by extraction with ethyl acetate
- filtrationThe organic layer was filtered through diatomaceous earth
- concentrationthe solvent was concentrated under reduced pressure
- customThe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=50:1→9:1)
出典と根拠
- ORDレコード
- ord-1d8f5338754f45f0bb6e0781d35a07a1
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822503B2
関連ノート
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