反応式
[NH2:1][C:2]([NH2:4])=[O:3].[CH2:5](N)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.N>>[CH2:5]([NH:1][C:2]([NH:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:3])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1参加物
4
実験手順
Heated was a mixture of urea 5.84 g (9.72 mmol) and benzylamine 25.0 g (23.3 mmol, 2.4 equivalents) at 150° C.-155° C. for 5 hours attaching with an air cooler. During the heating, observed was the ammonia gas evolution from colorless liquid reaction mixture. By cooling, it turned solidified at around room temperature. Purified was the reaction product by recrystallization from ethanol-benzene (1:1 mixture) to give N,N′-dibenzylurea 14.0 g as white fine needles (59.9% yield).
後処理
- temperatureHeated
- customfrom colorless liquid reaction mixture
- temperatureBy cooling
- customturned solidified at around room temperature
- customPurified
- customby recrystallization from ethanol-benzene (1:1 mixture)
出典と根拠
- ORDレコード
- ord-2828b789b1a44f70be3e7ce81ebdc615
- 出典データセット
- uspto-grants-2002_12
- 特許番号
- US06498164B1
関連ノート
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