N-[3-fluoro-2-(hydroxyl-o-tolyl-methyl)-phenyl]-acetamide → N-[3-fluoro-2-(2-methyl-benzoyl)-phenyl]-acetamide
反応式
[F:1][C:2]1[C:3]([CH:12]([OH:20])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[CH3:19])=[C:4]([NH:8][C:9](=[O:11])[CH3:10])[CH:5]=[CH:6][CH:7]=1>C(Cl)(Cl)Cl.[O-2].[Mn+4].[O-2]>[F:1][C:2]1[C:3]([C:12](=[O:20])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[CH3:19])=[C:4]([NH:8][C:9](=[O:11])[CH3:10])[CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
205 mg (0.75 mmol) N-[3-fluoro-2-(hydroxyl-o-tolyl-methyl)-phenyl]-acetamide are dissolved in 9 ml chloroform, combined with 652 mg (7.5 mmol) manganese(IV)-oxide and stirred for 3 d at ambient temperature. Then excess manganese(IV)-oxide is filtered off through Celite and the solvent is eliminated in vacuo. The crude product is purified by column chromatography. The carrier material used is silica gel and the eluant used is a mixture of cyclohexane:ethyl acetate (80:20).
後処理
- filtrationThen excess manganese(IV)-oxide is filtered off through Celite
- customThe crude product is purified by column chromatography
- additiona mixture of cyclohexane:ethyl acetate (80:20)
出典と根拠
- ORDレコード
- ord-0a32ff9d21694fd790aba529c9ff32d8
- 出典データセット
- uspto-grants-2007_07
- 特許番号
- US07241769B2
反応ノート
読み込み中…