反応式
[C:1]([C:4]1[CH:9]=[CH:8][N:7]=[CH:6][CH:5]=1)(=[O:3])[CH3:2].ClC1C=CC=C(C(OO)=[O:18])C=1>C(Cl)Cl>[C:1]([C:4]1[CH:9]=[CH:8][N+:7]([O-:18])=[CH:6][CH:5]=1)(=[O:3])[CH3:2]参加物
4
実験手順
The 4-acetyl-pyridine N-oxide used is prepared in the following manner: 11.0 ml (100 mmol) of 4-acetyl-pyridine and 31.3 g (100 mmol) of 55% m-chloro-perbenzoic acid are boiled under RF for 16 h in 200 ml of methylene chloride. Precipitation with 200 ml of diethyl ether gives 4-acetyl-pyridine N-oxide; m.p. 132°-133°.
後処理
- customThe 4-acetyl-pyridine N-oxide used is prepared in the following manner
- customPrecipitation with 200 ml of diethyl ether
出典と根拠
- ORDレコード
- ord-c9d27f69137047ca85c77482a3084a76
- 出典データセット
- uspto-grants-1998_03
- 特許番号
- US05728708
関連ノート
読み込み中…