Benzyl Chloride → N-Benzylcrotonamide
反応式
[C:1]([NH2:6])(=[O:5])/[CH:2]=[CH:3]/[CH3:4].[CH2:7](Cl)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>CN(C)C=O>[CH2:7]([NH:6][C:1](=[O:5])/[CH:2]=[CH:3]/[CH3:4])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1参加物
4
実験手順
To 200 ml of N,N-dimethylformamide, were added 17 g of crotonamide, 105 g of LEVATIT MP-500, which was also used in Example 68, and 32 g of benzylchloride. They were reacted at 50° C. for 4 hours with stirring. After the reaction, the reaction solution was treated in the same manner as in Example 69, the resulting distillation residue was recrystallized from benzine, and 25 of N-benzylcrotonamide having a melting point of 112.5°-113.6° C. was obtained (yield: 71%).
後処理
- customThey were reacted at 50° C. for 4 hours
- customAfter the reaction
- additionthe reaction solution was treated in the same manner as in Example 69
- distillationthe resulting distillation residue
- customwas recrystallized from benzine, and 25 of N-benzylcrotonamide having a melting point of 112.5°-113.6° C.
- customwas obtained (yield: 71%)
出典と根拠
- ORDレコード
- ord-0d5f89ffa64b4db3a7c5df88b628343f
- 出典データセット
- uspto-grants-1989_05
- 特許番号
- US04835312
反応ノート
読み込み中…