反応式
[CH3:1][N:2]([CH3:12])[C:3]1[CH:8]=[CH:7][C:6]([C:9](=[O:11])[CH3:10])=[CH:5][CH:4]=1>CN(C(OC)OC)C.C1(C)C=CC=CC=1.CC(O)=O>[CH3:1][N:2]([CH3:12])/[CH:3]=[CH:10]/[C:9]([C:6]1[CH:7]=[CH:8][C:3]([N:2]([CH3:1])[CH3:12])=[CH:4][CH:5]=1)=[O:11]参加物
5
実験手順
A solution of 1-[4-(dimethylamino)phenyl]ethanone (500 mg, 3.1 mmol) in DMF-DMA (10 mL), toluene (10 mL), and AcOH (2 drops), was heated under reflux conditions for 48 h. The solution was concentrated and purified by flash column chromatography (hexanes:EtOAc=8:2˜1:1) to give the title compound (121 mg, 18%) as a yellow solid.
後処理
- concentrationThe solution was concentrated
- custompurified by flash column chromatography (hexanes:EtOAc=8:2˜1:1)
出典と根拠
- ORDレコード
- ord-902f43f21db94618b0be5351002cdefa
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09107916B2
関連ノート
読み込み中…