HRID1926718

反应详情

EQUATION

反应方程式

HRID 1926718 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
121 °C

PROCEDURE

实验过程

2-(Trifluoromethyl)-1,4,5,6-tetrahydropyrimidin-5-ol (4.20 g, 25 mmol) was stirred in nitrobenzene at 90° C. Sodium methoxide (5.4 g, 100 mmol) was dissolved in methanol (75 ml) and added portionwise to the reaction mixture, allowing the methanol to distill off before the next addition. The reaction mixture was then warmed to 121° C. for one hour, cooled, shaken with water (150 ml), the organic phase separated off and the aqueous phase washed with ethyl acetate (2×100 ml). The aqueous phase was adjusted to pH 4.0 with 6M aqueous hydrochloric acid, extracted with ethyl acetate (2×100 ml), dried and evaporated to give 2.53 g (61.7%) of an orange coloured product that was used without further purification.

WORKUP

后处理

  1. additionadded portionwise to the reaction mixture
  2. distillationto distill off before the next addition
  3. temperaturecooled
  4. customthe organic phase separated off
  5. washthe aqueous phase washed with ethyl acetate (2×100 ml)
  6. extractionextracted with ethyl acetate (2×100 ml)
  7. customdried
  8. customevaporated