HRID2410235

反应详情

EQUATION

反应方程式

HRID 2410235 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

N-(2-Fluorophenyl)-N′-[2-methoxy-5-(trifluoromethyl)phenyl]urea (0.225 kg) is dissolved in acetic acid (6.75 l) and treated with palladium acetate (30.3 g). 65% strength oleum (247.5 g) is then metered in and methyl acrylate (90 g) is subsequently added. The solution is stirred at room temperature overnight. Subsequently, acetic acid (3740 g) is distilled off at 30° C. and ca. 30 mbar. The suspension is treated with water (2.25 l) and stirred for ca. 1 hour. The product is filtered off with suction, washed twice with water (0.5 l) and dried at 50° C. overnight in the vacuum drying oven using entraining nitrogen. A total of 210.3 g of methyl (2E)-3-{3-fluoro-2-[({[2-methoxy-5-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenyl}acrylate are obtained as a solid, corresponding to 72.2% of theory.

WORKUP

后处理

  1. additionis subsequently added
  2. distillationSubsequently, acetic acid (3740 g) is distilled off at 30° C.
  3. additionThe suspension is treated with water (2.25 l)
  4. stirringstirred for ca. 1 hour
  5. filtrationThe product is filtered off with suction
  6. washwashed twice with water (0.5 l)
  7. customdried at 50° C. overnight in the vacuum
  8. customdrying oven