Ammonia → 1-(Dimethylamino)-3-(thiophen-2-yl)propan-2-one
反応式
[C:1]([C:4]1[S:5][CH:6]=[CH:7][CH:8]=1)(=O)C.C=O.Cl.[CH3:12][NH:13][CH3:14].Cl.N.[CH2:17]([OH:19])[CH3:18]>>[CH3:12][N:13]([CH3:14])[CH2:18][C:17](=[O:19])[CH2:1][C:4]1[S:5][CH:6]=[CH:7][CH:8]=1参加物
7
実験手順
The synthesis of 2,5-Di-(2-thienyl)-pyrrole and N-substituted derivatives thereof is shown in FIG. 3. 3-dimethylamino-1-(2-thienyl)-propanone hydrochloride (4) is produced in 89% yield by refluxing for 16 hours a mixture of 2-acetylthiophene (1), paraformaldehyde (2), dimethylamine hydrochloride (3) and concentrated hydrochloric acid in ethanol. The product is isolated, treated with 35% aqueous ammonia and extracted with ether to yield 3-dimethylamino-1-(2-thienyl)-propanone (5).
後処理
- temperatureby refluxing for 16 hours
- customThe product is isolated
- extractionextracted with ether
出典と根拠
- ORDレコード
- ord-c6f040bb3ecd42b69591bcb84688511c
- 出典データセット
- uspto-grants-2001_01
- 特許番号
- US06180064B2
反応ノート
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