反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[O:15]1[CH:19]=[CH:18][CH:17]=[C:16]1[C:20](Cl)=[O:21]>ClCCl>[C:2]1([NH:1][C:20]([C:16]2[O:15][CH:19]=[CH:18][CH:17]=2)=[O:21])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
5
反応条件
- 温度
- -10 °C
実験手順
N-phenyl furamide was prepared by adding to a mixture of aniline (23.3 g; 250 mmol) and triethylamine (25.3 g; 250 mmol) in dichloromethane slowly 32.6 g (250 mmol) of 2-furoyl chloride, while maintaining the temperature at -10° C. The product obtained was washed with diluted hydrochloric acid and water, dried with magnesium sulphate and evaporated. The product so obtained was than triturated with hexane and filtered. 39.3 g (84% yield of product was recovered.
後処理
- customThe product obtained
- washwas washed with diluted hydrochloric acid and water
- dry with materialdried with magnesium sulphate
- customevaporated
- customThe product so obtained
- customthan triturated with hexane
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-ec294cbabf8b4576be6a8b4d93a811ec
- 出典データセット
- uspto-grants-1999_07
- 特許番号
- US05925152
関連ノート
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