Benzocaine → Ethyl 4-(2,5-dimethyl-1H-pyrrol-1-yl)benzoate
反応式
[CH2:1]([O:3][C:4]([C:6]1[CH:12]=[CH:11][C:9]([NH2:10])=[CH:8][CH:7]=1)=[O:5])[CH3:2].[CH2:13]([CH2:17][C:18](=O)[CH3:19])[C:14]([CH3:16])=O>S(=O)(=O)(O)O.C(OCC)(=O)C>[CH2:1]([O:3][C:4]([C:6]1[CH:12]=[CH:11][C:9]([N:10]2[C:18]([CH3:19])=[CH:17][CH:13]=[C:14]2[CH3:16])=[CH:8][CH:7]=1)=[O:5])[CH3:2]参加物
5
反応条件
- 温度
- 150 °C
実験手順
A mixture of 4-ethoxycarbonylaniline (82.6 g), acetonylacetone (68.5 g) and concentrated sulfuric acid (one drop) were heated at 150° C. for one hour. The reaction mixture was diluted with ethyl acetate and washed with water, followed by drying and concentrating, whereby 1-(4-ethoxycarbonylphenyl)-2,5-dimethylpyrrole was obtained.
後処理
- washwashed with water
- customby drying
- concentrationconcentrating
出典と根拠
- ORDレコード
- ord-a10ef2ba104c469b8c46bd7bde4a3067
- 出典データセット
- uspto-grants-1994_03
- 特許番号
- US05296344
反応ノート
読み込み中…