反応式
[NH:1]1[CH2:7][C:5](=[O:6])[NH:4][C:2]1=[O:3].BrBr.[C:10]1([O:16][CH3:17])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>C(O)(=O)C>[CH3:17][O:16][C:10]1[CH:15]=[CH:14][C:13]([CH:7]2[NH:1][C:2](=[O:3])[NH:4][C:5]2=[O:6])=[CH:12][CH:11]=1参加物
5
反応条件
- 温度
- 60 °C
実験手順
4.0 g (40 mmol) of hydantoin, 30 ml of acetic acid and 2.0 ml (40 mmol) of bromine were mixed at room temperature. The reaction mixture was then vigorously stirred at a temperature of 60° C. for 2 hours. After cooling the reaction mixture to room temperature, 8.64 g (80 mmol) of anisol was added to the reaction mixture and the reaction was further conducted at a temperature of 100° C. for 6 hours. The resulting precipitate was recovered by filtration, washed with water, and then dried to obtain 3.96 g (yield 48%) of 5-(p-methoxyphenyl)hydantoin.
後処理
- temperatureAfter cooling the reaction mixture to room temperature
- waitthe reaction was further conducted at a temperature of 100° C. for 6 hours
- filtrationThe resulting precipitate was recovered by filtration
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-ef6827e3c6114e9099ec6e224c87bb65
- 出典データセット
- uspto-grants-1997_02
- 特許番号
- US05606071
関連ノート
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