Hydrochloric Acid → 5-Chloro-2-((2-chloroacetyl)amino)benzoic acid
反応式
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[Cl:12][CH2:13][C:14](Cl)=[O:15].C(=O)([O-])[O-].[K+].[K+].Cl>C(#N)C>[Cl:12][CH2:13][C:14]([NH:1][C:2]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5])=[O:15]参加物
実験手順
12.5 g (73 mmol) of 2-amino-5-chlorobenzoic acid are initially introduced into 500 ml of acetonitrile and treated with 9.0 g (80 mmol) of chloroacetyl chloride with stirring, the temperature being kept at 20°-25° C. (ice-bath). 22 g (0.16 mol) of finely pulverized potassium carbonate are then introduced and the mixture is stirred overnight at room temperature. The batch is adjusted to pH 2 with dilute hydrochloric acid and the acetonitrile is stripped off on a rotary evaporator. The precipitate is filtered off with suction and washed well with water. The crude product is treated with sodium bicarbonate solution and stirred. Insoluble matter is filtered off with suction and the filtrate acidified with dilute hydrochloric acid to pH 2. The precipitated product is filtered off with suction and dried. Yield: 7 g (77.3% of theory) M.p.: 188° C.
後処理
- custombeing kept at 20°-25° C.
- stirringthe mixture is stirred overnight at room temperature
- customthe acetonitrile is stripped off on a rotary evaporator
- filtrationThe precipitate is filtered off with suction
- washwashed well with water
- additionThe crude product is treated with sodium bicarbonate solution
- stirringstirred
- filtrationInsoluble matter is filtered off with suction
- filtrationThe precipitated product is filtered off with suction
- customdried
出典と根拠
- ORDレコード
- ord-a1de311ebc264719961cf4cbd214c1b8
- 出典データセット
- uspto-grants-1996_11
- 特許番号
- US05571921
反応ノート
読み込み中…