Potassium Iodide → HCID 20402707、化合物
反応式
[C:1]([C:9]1[C:10]([NH:16][C:17](=[O:20])[CH2:18]Cl)=[CH:11][N:12]([CH3:15])[C:13]=1[CH3:14])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[I-:21].[K+]>C(O)C>[C:1]([C:9]1[C:10]([NH:16][C:17](=[O:20])[CH2:18][I:21])=[CH:11][N:12]([CH3:15])[C:13]=1[CH3:14])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
4
実験手順
N-(4-benzoyl-1,5-dimethyl(1H)pyrrol-3-yl)2-chloroacetamide (0.741 mole) and potassium iodide (1.62 mole) were refluxed in ethanol (3400 ml) for 5 hours with stirring. The reaction mixture was then cooled, the inorganic salts were filtered off and the solvent was evaporated under vacuum. The obtained residue was purified by washing first with water and then with cold ethanol. M.p. 135°-137° C. Yield 87%.
後処理
- temperatureThe reaction mixture was then cooled
- filtrationthe inorganic salts were filtered off
- customthe solvent was evaporated under vacuum
- customThe obtained residue was purified
- washby washing first with water
出典と根拠
- ORDレコード
- ord-5b0c6240e9054f30a69c9a3fee9ae5b8
- 出典データセット
- uspto-grants-1983_09
- 特許番号
- US04402970
反応ノート
読み込み中…