Pyridine → 1-o-Tolyl-propane-1,2-dione
反応式
[C:1]1([CH3:11])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][C:8](=[O:10])[CH3:9].[Cr](Cl)([O-])(=O)=[O:13].[NH+]1C=CC=CC=1.N1C=CC=CC=1>C(Cl)Cl>[C:1]1([CH3:11])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7](=[O:13])[C:8](=[O:10])[CH3:9]参加物
5
実験手順
A mixture of 7 g (47.23 mmol) 1-o-Tolyl-propan-2-one, 30.5 g (0.141 mol) pyridinium chlorochromate and 11.2 g (0.141 mol) pyridine in 200 ml DCM was heated to reflux for 16 h. The mixture was filtered through a pad of silica and the filtrate was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica eluting with ethyl acetate/n-hexane 1:4. The product fractions were evaporated to yield 1.178 g (15%) of the title compound.
後処理
- temperaturewas heated
- temperatureto reflux for 16 h
- filtrationThe mixture was filtered through a pad of silica
- customthe filtrate was evaporated under reduced pressure
- customThe residue was purified by flash column chromatography on silica eluting with ethyl acetate/n-hexane 1:4
- customThe product fractions were evaporated
出典と根拠
- ORDレコード
- ord-d3283aa22633440c9c72b26f773945fc
- 出典データセット
- uspto-grants-2004_02
- 特許番号
- US06686381B2
反応ノート
読み込み中…