反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N+:3]=1[O-].CC[O:11][C:12]([CH3:14])=[O:13]>C(OC(=O)C)(=O)C>[C:12]([O:13][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1)(=[O:11])[CH3:14]参加物
4
実験手順
A solution of the 2-methyl pyridine N-oxide (1.0 mmol) in acetic anhydride (5 mL) 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-4d43528ff4754e27a402addcc765c256
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- US07148228B2
関連ノート
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