Imidazole → 4-(4-Chlorophenyl)-1-(imidazol-1-yl)butan-2-one
反応式
Cl[CH2:2][C:3](=[O:13])[CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([Cl:12])=[CH:8][CH:7]=1.[NH:14]1[CH:18]=[CH:17][N:16]=[CH:15]1.O>CN(C)C=O>[Cl:12][C:9]1[CH:10]=[CH:11][C:6]([CH2:5][CH2:4][C:3](=[O:13])[CH2:2][N:14]2[CH:18]=[CH:17][N:16]=[CH:15]2)=[CH:7][CH:8]=1参加物
5
実験手順
1-Chloro-4-(4-chlorophenyl)-2-butanone (110 g) was added portionwise over half an hour to a stirred suspension of imidazole (175 g) in dimethylformamide (150 ml) at 0° C. and the mixture stirred overnight at ambient temperature. The resulting solution was poured into water (1500 ml) with seeding at the first sign of turbidity, and the precipitate filtered off and washed well with water and hexane. Chromatography of the product on silica gel (1 Kg.), eluting with 7% methanol in methylene chloride gave 100 g of 1-[4-(4-chlorophenyl)butan-2-on-1-yl]imidazole.
後処理
- filtrationthe precipitate filtered off
- washwashed well with water and hexane
- washChromatography of the product on silica gel (1 Kg.), eluting with 7% methanol in methylene chloride
出典と根拠
- ORDレコード
- ord-7b869343bf794572aeabfe544ed4dde3
- 出典データセット
- uspto-grants-1983_03
- 特許番号
- US04375474
反応ノート
読み込み中…