反応式
[OH-:1].[Na+].[OH2:3].O[C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][CH:14]=1)[N:11]=[CH:10][CH:9]=[CH:8]2.[CH:15](Cl)(Cl)Cl>>[OH:1][C:5]1[CH:14]=[CH:13][C:12]2[N:11]=[CH:10][CH:9]=[CH:8][C:7]=2[C:6]=1[CH:15]=[O:3]参加物
5
反応条件
- 温度
- 90 °C
実験手順
Sodium hydroxide (25 g.) was dissolved in 35 ml. of water with cooling, 6-hydroxyquinoline (5 g.) in 15 ml. of chloroform was added and the reaction mixture heated to reflux (about 90° C.) for 12 hours, during which two further 15 ml. portions of chloroform were added--one after 2 hours and the other after 6 hours. The reaction mixture was cooled and crude product recovered by filtration. The crude was dissolved in 125 ml. of hot water treated with activated carbon, filtered hot, cooled and acidified with acetic acid and filtered to yield title product [2.5 g.; m.p 136°-137° C.; m/e 173; pnmr/CDCl3 shows aldehyde proton at 10.5 ppm and aromatic protons at 7.2-9.4 ppm⟧
後処理
- temperaturethe reaction mixture heated
- waitthe other after 6 hours
- temperatureThe reaction mixture was cooled
- filtrationcrude product recovered by filtration
- dissolutionThe crude was dissolved in 125 ml
- additionof hot water treated with activated carbon
- filtrationfiltered hot
- temperaturecooled
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-12a8023b7b894ac3bb091ca882f9c9db
- 出典データセット
- uspto-grants-1982_08
- 特許番号
- US04342771
関連ノート
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