3-[4-(1h-Pyrazol-1-yl)phenyl]-2-propyn-1-ol → 3-[4-(1H-pyrazol-1-yl)phenyl]-2-propynal
反応式
[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([C:12]#[C:13][CH2:14][OH:15])=[CH:8][CH:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1>CC(C)=O.O=[Mn]=O>[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([C:12]#[C:13][CH:14]=[O:15])=[CH:8][CH:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1参加物
4
実験手順
A mixture of the compound from step A (0.71 g, 3.58 mmol) and MnO2 (3.10 g, 35.66 mmol) in acetone (40 mL) was heated to reflux for 3 h. The cooled reaction mixture was filtered through Celite and the filtrate was concentrated. Purification by chromatography (SiO2, 6:1 hexane/ethyl acetate) yielded 0.19 g (27%) of the title compound as an off-white solid. MS 197 (M+H)+.
後処理
- temperaturewas heated
- temperatureto reflux for 3 h
- customThe cooled reaction mixture
- filtrationwas filtered through Celite
- concentrationthe filtrate was concentrated
- customPurification by chromatography (SiO2, 6:1 hexane/ethyl acetate)
出典と根拠
- ORDレコード
- ord-e86d5d11c86c4fb1b2b5701a97a123d5
- 出典データセット
- uspto-grants-2004_11
- 特許番号
- US06825170B2
反応ノート
読み込み中…