反应 #84047

反应方程式

barbituric acid

3,5-dibromo-2-hydroxybenzaldehyde

→

product 1a

收率 84.6%

5-(3,5-dibromo-2-hydroxybenzylidene) perhydropyrimidine-2,4,6-trione

收率 84.6%

溶剂

acetic acid

反应条件

后处理

1. 1
   温度while heating
2. 2
   其他the resulting reaction mixture
3. 3
   过滤The produced crystal product was filtered
4. 4
   洗涤washed with cold acetic acid
5. 5
   洗涤washed with ether
6. 6
   其他air-dried

实验过程

0.01 mol (1.28 g) of barbituric acid (5a) were dissolved in 25 ml of glacial acetic acid while heating. Then 0.011 mol (3.08 g) of 3,5-dibromo-2-hydroxybenzaldehyde (6a) were added to the obtained solution while stirring and the resulting reaction mixture was left at room temperature during 36 hours. The produced crystal product was filtered, washed with cold acetic acid, then washed with ether and air-dried. Thereby 3.3 g of product 1a were obtained in the form of yellow needle crystals with melting temperature of 255-260° C. (with decomposition). Output amounted to 77% of the theoretical value.

来源