Hydrogen Bromide → 1-(3-Bromopropyl)-5-chloro-1,3-dihydro-2H-benzimidazol-2-one
反応式
[Cl:1][C:2]1[CH:15]=[CH:14][C:5]2[N:6]([CH2:10][CH2:11][CH2:12]O)[C:7](=[O:9])[NH:8][C:4]=2[CH:3]=1.[BrH:16]>O>[Br:16][CH2:12][CH2:11][CH2:10][N:6]1[C:5]2[CH:14]=[CH:15][C:2]([Cl:1])=[CH:3][C:4]=2[NH:8][C:7]1=[O:9]参加物
実験手順
A mixture of 9.3 parts of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one and 83 parts of a hydrobromic acid solution 48% in water was stirred and refluxed for 6 hours. The reaction mixture was cooled and allowed to crystallize overnight at room temperature. The precipitated product was filtered off and stirred a few times in 100 parts of water till the pH of the filtrate was greater than 2. The product was stirred and refluxed for 1 hour in 55 parts of chlorobenzene with 1.3 parts of activated charcoal. The latter was filtered off and the filtrate was allowed to crystallize overnight in an ice-box. The product was filtered off and recrystallized twice: first from chlorobenzene (activated charcoal) and then from methylbenzene (activated charcoal), yielding 4.9 parts of 1-(3-bromopropyl)-5-chloro-1,3-dihydro-2H-benzimidazol-2-one; mp. 161.5° C. (intermediate 29).
後処理
- temperaturerefluxed for 6 hours
- temperatureThe reaction mixture was cooled
- customto crystallize overnight at room temperature
- filtrationThe precipitated product was filtered off
- stirringstirred a few times in 100 parts of water till the pH of the filtrate
- stirringThe product was stirred
- temperaturerefluxed for 1 hour in 55 parts of chlorobenzene with 1.3 parts of activated charcoal
- filtrationThe latter was filtered off
- customto crystallize overnight in an ice-box
- filtrationThe product was filtered off
- customrecrystallized twice
出典と根拠
- ORDレコード
- ord-074845c1bc8d449aa38b1c8ff77bae3e
- 出典データセット
- uspto-grants-1992_08
- 特許番号
- US05137896
反応ノート
読み込み中…