Hydrogen Peroxide → Pyridine, 3-(phenylmethyl)-, 1-oxide
反応式
[CH2:1]([C:8]1[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH:14]O>C(O)(=O)C>[CH2:1]([C:8]1[CH:9]=[N+:10]([O-:14])[CH:11]=[CH:12][CH:13]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
A solution of 3-benzylpyridine (25 g, 0.148 tool) in hydrogen peroxide (30%, 15.1 mL) and acetic acid (100 mL) was refluxed for one day. Then more hydrogen peroxide (3 mL) was added and the resulting mixture was refluxed overnight. The reaction mixture was then evaporated and partitioned between a mixture of 3 N HCl, brine and dichloromethane. The organic layer was separated, dried and evaporated to give the desired compound (27.6 g, 100%).
後処理
- temperaturethe resulting mixture was refluxed overnight
- customThe reaction mixture was then evaporated
- custompartitioned between a mixture of 3 N HCl, brine and dichloromethane
- customThe organic layer was separated
- customdried
- customevaporated
出典と根拠
- ORDレコード
- ord-3e12e8445c50462ea540c0fda3bb7416
- 出典データセット
- uspto-grants-1996_02
- 特許番号
- US05494919
反応ノート
読み込み中…