Pyridine → 1-(2-Oxo-2-phenylethyl)pyridin-1-ium bromide
反応式
[CH2:1]([Br:10])[C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[O:3].[N:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[Br-:10].[CH2:1]([N+:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[O:3]参加物
3
実験手順
N-phenacylpyridinium bromide was prepared by slowly adding phenacyl bromide to a stirred flask containing an equimolar quantity of pyridine. The slightly exothermic reaction was accompanied by the precipitation of the solid N-phenacylpyridinium bromide. The salt was then filtered and washed thoroughly with anhydrous ether.
後処理
- customThe slightly exothermic reaction
- customwas accompanied by the precipitation of the solid N-phenacylpyridinium bromide
- filtrationThe salt was then filtered
- washwashed thoroughly with anhydrous ether
出典と根拠
- ORDレコード
- ord-fdd250d095a145258c404b131ea85838
- 出典データセット
- uspto-grants-1978_01
- 特許番号
- US04069055
反応ノート
読み込み中…