HRID616535

反应详情

EQUATION

反应方程式

HRID 616535 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
40 °C

PROCEDURE

实验过程

19.6 g of 2,4,6-triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidine and 0.4 g of ammonium bromide were added to 200 ml of methanol. To the mixture were added dropwise 10 g of a 37% aqueous hydrochloric acid solution at 10° C, with stirring. When the addition was complete, the whole mixture was stirred at room temperature for 4 hours, after which 20 ml of 18% aqueous hydrochloric acid were then added. The mixture was then heated at 30' - 40° C for 7 hours and allowed to stand overnight at room temperature. The resulting mixture was made alkaline by addition of a 40% aqueous solution of potassium carbonate and, after evaporating off the methanol under reduced pressure, the mixture was extracted with diethyl ether. The ethereal extract was dried over potassium carbonate, after which the diethyl ether was removed. The residue was then distilled under reduced pressure, giving 15.1 g of the title compound as an oil boiling at 91° - 93° C/2.0 mmHg.

WORKUP

后处理

  1. additionWhen the addition
  2. stirringthe whole mixture was stirred at room temperature for 4 hours
  3. customafter evaporating off the methanol under reduced pressure
  4. extractionthe mixture was extracted with diethyl ether
  5. extractionThe ethereal extract
  6. dry with materialwas dried over potassium carbonate
  7. customafter which the diethyl ether was removed
  8. distillationThe residue was then distilled under reduced pressure