Sodium Hydroxide → 8-Hydroxyquinoline
反応式
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2S([O-])(=O)=O)[CH:4]=[CH:3][CH:2]=1.[Na+].[OH-:16].[Na+]>O>[OH:16][C:9]1[CH:8]=[CH:7][CH:6]=[C:5]2[C:10]=1[N:1]=[CH:2][CH:3]=[CH:4]2参加物
4
実験手順
Sodium quinoline-8-sulfonate (231 g) was added to 170 g of a 50% aqueous solution of sodium hydroxide, and the mixture was stirred. Then, 900 g of a hydrogenated triphenyl mixture was mixed, and the mixture was dehydrated. The dehydrated mixture was reacted at 260° C. for 15 minutes in a nitrogen stream. After cooling, 600 ml of water was added to the reaction mixture to separate the reaction medium layer. The aqueous layer was decolorized with activated carbon, acidified and then extracted with 200 ml of chloroform. The chloroform was recovered to give 140.9 g (yield 97.2%) of 8-hydroxyquinoline.
後処理
- customThe dehydrated mixture was reacted at 260° C. for 15 minutes in a nitrogen stream
- temperatureAfter cooling
- customto separate the reaction medium layer
- extractionextracted with 200 ml of chloroform
- customThe chloroform was recovered
出典と根拠
- ORDレコード
- ord-598777ab442c45c7ac24497548efd2a9
- 出典データセット
- uspto-grants-1986_12
- 特許番号
- US04633024
反応ノート
読み込み中…