Ammonia → 3,5-Dichloro-2-hydroxybenzamide
反応式
[Cl:1][C:2]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:4]([C:5](OC)=[O:6])[C:3]=1[OH:13].[NH3:14]>>[Cl:1][C:2]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:4]([C:5]([NH2:14])=[O:6])[C:3]=1[OH:13]参加物
3
反応条件
- 温度
- 25 °C
実験手順
A 1 liter Parr autoclave was charged with 221 g. (1 mole) -dichlorophenyl)- of methyl 3,5-dichlorosalicylate and 140 g. (8 moles) of anhydrous ammonia. The mixture was stirred at 25° C for 24 hours. After venting excess ammonia, the product was ground to a fine powder and triturated with boiling chloroform. The mixture was filtered while hot and the residue weighed 153 g. Analysis by infrared, gas chromatography, and nuclear magnetic resonance confirmed that the product was 3,5-dichlorosalicylamide.
後処理
- additionA 1 liter Parr autoclave was charged with 221 g
- customtriturated with boiling chloroform
- filtrationThe mixture was filtered while hot and the residue
出典と根拠
- ORDレコード
- ord-a66591768d304c25bc90ad70e522d405
- 出典データセット
- uspto-grants-1977_04
- 特許番号
- US04020081
反応ノート
読み込み中…