反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N+:3]=1[O-].[C:9]([O:12]C(=O)C)(=[O:11])[CH3:10]>CCOC(C)=O>[C:9]([O:12][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1)(=[O:11])[CH3:10]参加物
4
実験手順
A solution of the 2-methyl pyridine N-oxide (1.0 mmol) in acetic anhydride (5 mmol) was heated to reflux for 0.5 h. Work-up (EtOAc), drying (MgSO4), evaporation and purification by preparative TLC or flash chromatography afforded the 2-(acetoxymethyl)pyridine.
後処理
- temperatureto reflux for 0.5 h
- customdrying
- custom(MgSO4), evaporation and purification by preparative TLC or flash chromatography
出典と根拠
- ORDレコード
- ord-46b932fbdc8540ac87584522c6800eb6
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07138401B2
関連ノート
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