3,4-dihydro-2H-pyrano[2,3-c]pyridin-6-ylmethanol → 3,4-dihydro-2H-pyrano[2,3-c]pyridine-6-carbaldehyde
反応式
[O:1]1[C:6]2=[CH:7][N:8]=[C:9]([CH2:11][OH:12])[CH:10]=[C:5]2[CH2:4][CH2:3][CH2:2]1>C(Cl)(Cl)Cl.[O-2].[O-2].[Mn+4]>[O:1]1[C:6]2=[CH:7][N:8]=[C:9]([CH:11]=[O:12])[CH:10]=[C:5]2[CH2:4][CH2:3][CH2:2]1参加物
4
実験手順
To a solution of 0.25 g of (3,4-dihydro-2H-pyrano(2,3-c)pyridin-6-yl)methanol in 7.5 mL of chloroform, 0.66 g of manganese dioxide was added, and the mixture was heated under reflux while stirring for 4 hours 50 minutes. The reaction mixture was cooled to room temperature, the insoluble substance was then filtered off, and the solvent was distilled off under reduced pressure to obtain 0.24 g of 3,4-dihydro-2H-pyrano(2,3-c)pyridine-6-carbaldehyde as a light yellow oily substance.
後処理
- temperaturethe mixture was heated
- temperatureunder reflux
- filtrationthe insoluble substance was then filtered off
- distillationthe solvent was distilled off under reduced pressure
出典と根拠
- ORDレコード
- ord-42bb9524deb642bc8debad7f04403bb2
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08367831B2
反応ノート
読み込み中…