反応式
[NH:1]([C:5]1[CH:10]=[CH:9][C:8]([C:11](=[O:15])[CH2:12][CH2:13][CH3:14])=[CH:7][CH:6]=1)C(C)=O.[OH-].[Na+]>Cl>[NH2:1][C:5]1[CH:6]=[CH:7][C:8]([C:11](=[O:15])[CH2:12][CH2:13][CH3:14])=[CH:9][CH:10]=1参加物
4
実験手順
20 g of p-acetaminobutyrophenone are suspended in 40 ml of semi-concentrated hydrochloric acid and the suspension is heated under reflux for 25 minutes and poured into a mixture of 100 ml of ice and 30 ml of concentrated sodium hydroxide solution. The mixture is filtered with suction, then the residue is washed twice with ice-cold water, dried in the atmosphere and recrystallised from methanol/water (20 ml+100 ml). p-Aminobutyrophenone having a melting point of 93°-94° is obtained.
後処理
- temperaturethe suspension is heated
- temperatureunder reflux for 25 minutes
- filtrationThe mixture is filtered with suction
- washthe residue is washed twice with ice-cold water
- customdried in the atmosphere
- customrecrystallised from methanol/water (20 ml+100 ml)
出典と根拠
- ORDレコード
- ord-c84a30cb5b8e46ada567659ae69b8810
- 出典データセット
- uspto-grants-1984_10
- 特許番号
- US04476132
関連ノート
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