反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The starting material was prepared as follows. 4-Amino-2-bromothiazole (15.6 g) and chloroacetyl chloride (7.6 g) were suspended in methylene chloride (100 ml) with stirring and treated with pyridine (16 ml) over 15 min., maintaining reaction temperature at 0° C. with an ice bath. After the addition was complete, the reaction mixture was stirred at room temperature for 3 hours, then poured onto 20% aqueous sodium acetate (500 ml) and stirred for 30 minutes. The mixture was separated and the organic layer washed with 2N hydrochloric acid, water, sodium carbonate solution and water. The organic layer was dried (MgSO4) and the solvent removed in vacuo and the residue recrystallised twice from carbon tetrachloride to give 2-bromo-4-chloroacetamidothiazole (5.1 g). m.p. 146°-8° C. (Found: C, 24.1; H, 1.7; N, 11.2. C5H4ClBrN2OS requires C, 23.5; H, 1.6; N, 11.0%).
WORKUP
后处理
- customThe starting material was prepared
- temperaturemaintaining
- customreaction temperature at 0° C. with an ice bath
- additionAfter the addition
- stirringthe reaction mixture was stirred at room temperature for 3 hours
- stirringstirred for 30 minutes
- customThe mixture was separated
- washthe organic layer washed with 2N hydrochloric acid, water, sodium carbonate solution and water
- dry with materialThe organic layer was dried (MgSO4)
- customthe solvent removed in vacuo
- customthe residue recrystallised twice from carbon tetrachloride