HRID126879

反应详情

EQUATION

反应方程式

HRID 126879 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

17 g (0.05 mol) of crude 1-bromo-1-(4-chlorophenoxy)-3,3-dimethyl-4-chloro-butan-2-one were dissolved in 100 ml of absolute acetonitrile. 12 g (0.175 mol) of imidazole were added to this solution and the mixture was heated under reflux for 40 hours. Thereafter, it was concentrated by distilling off the solvent in vacuo and the residue was taken up in 300 ml of methylene chloride. The methylene chloride mixture was washed three times with 100 ml of water each time, dried over sodium sulphate and concentrated again in vacuo. The residue was taken up in 100 ml of acetone, and a solution of 9 g (0.038 mol) of 1,5-naphthalenedisulphonic acid in 50 ml of acetone was added. After 2 hours, the precipitate which had formed was filtered off and dried. 19.8 g (80.7% of theory) of 1-(4-chlorophenoxy)-1-(imidazol-1-yl)-3,3-dimethyl-4-chloro-butan-2-one naphthalene-1,5-disulphonate of melting point 266°- 267° C. were obtained. ##STR14##

WORKUP

后处理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 40 hours
  3. concentrationThereafter, it was concentrated
  4. distillationby distilling off the solvent in vacuo
  5. washThe methylene chloride mixture was washed three times with 100 ml of water each time
  6. dry with materialdried over sodium sulphate
  7. concentrationconcentrated again in vacuo
  8. customthe precipitate which had formed
  9. filtrationwas filtered off
  10. customdried