反応式
[NH2:1][C:2]1[C:10]([CH:11]=[N:12][O:13][CH3:14])=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[Cl:15].C1(C)C=CC=CC=1.S(Cl)([Cl:25])=O>CN(C)C=O>[NH2:1][C:2]1[C:10]([CH:11]=[N:12][O:13][CH3:14])=[CH:9][C:5]([C:6]([Cl:25])=[O:7])=[CH:4][C:3]=1[Cl:15]参加物
5
反応条件
- 温度
- 70 °C
実験手順
In a 5-liter three-necked round-bottomed flask was placed 180 g of the previously prepared 4-amino-3-chloro-5-methoxyiminomethylbenzoic acid, 2 l of toluene, 3 mL of dimethylformamide and 104 g (64 mL) of thionyl chloride. The resulting mixture was heated at 70° C. for 2 hours, filtered while hot and the solvent removed using a rotary evaporator yielding 178.1 g of the expected 4-amino-3-chloro-5-methoxyiminomethylbenzoyl chloride.
後処理
- customIn a 5-liter three-necked round-bottomed flask was placed
- filtrationfiltered while hot and the solvent
- customremoved
- customa rotary evaporator
出典と根拠
- ORDレコード
- ord-d37d0d004e6b4141a4e103e2f0b98b0f
- 出典データセット
- uspto-grants-2000_10
- 特許番号
- US06140362
関連ノート
読み込み中…