Acetic Anhydride → (4-Chloro-6-methylpyridin-2-yl)methyl acetate
反応式
[Cl:1][C:2]1[CH:7]=[C:6]([CH3:8])[N+:5]([O-])=[C:4]([CH3:10])[CH:3]=1.[C:11]([O:14]C(=O)C)(=[O:13])[CH3:12]>>[Cl:1][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]([CH2:10][O:14][C:11](=[O:13])[CH3:12])[CH:3]=1参加物
3
実験手順
4.0 g (25.4 mmol) of 4-chloro-2,6-dimethylpyridine-1-oxide was dissolved in 12 ml of acetic anhydride. The resultant solution was gradually heated to raise the temperature to the reflux temperature, and the solution was then stirred overnight at the same temperature. The reacted solution was then condensed under reduced pressure to obtain a crude product of acetic 4-chloro-6-methyl-2-pyridinylmethyl ester.
後処理
- temperatureto raise the temperature to the reflux temperature
- customcondensed under reduced pressure
出典と根拠
- ORDレコード
- ord-b874bf9cc70649c696331d3670e0b7f4
- 出典データセット
- uspto-grants-2003_07
- 特許番号
- US06589967B1
反応ノート
読み込み中…