Hydrochloric Acid → 4-(Pyridin-3-YL)benzoic acid hydrochloride
反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[CH:16]=[CH:15][C:10]([C:11]([O:13]C)=[O:12])=[CH:9][CH:8]=2)[CH:2]=1.[ClH:17]>O1CCOCC1>[ClH:17].[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[CH:16]=[CH:15][C:10]([C:11]([OH:13])=[O:12])=[CH:9][CH:8]=2)[CH:2]=1参加物
4
実験手順
At room temperature, methyl 4-(3-pyridyl)benzoate (1.76 g) was dissolved in a mixed solvent of 1N hydrochloric acid (50 ml) and dioxane (50 ml), followed by heating under reflux for 4 hours. The solvent was then distilled off under reduced pressure. Tetrahydrofuran was added to the residue, followed by washing, whereby the title compound (1.55 g, 93%) was obtained as a colorless solid.
後処理
- temperatureby heating
- temperatureunder reflux for 4 hours
- distillationThe solvent was then distilled off under reduced pressure
- additionTetrahydrofuran was added to the residue
- washby washing
出典と根拠
- ORDレコード
- ord-2eb6859311e1444da9afb28c8ff56524
- 出典データセット
- uspto-grants-2004_06
- 特許番号
- US06747023B1
反応ノート
読み込み中…