HRID746275

反应详情

EQUATION

反应方程式

HRID 746275 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

1.53 g (0.005 mole) of methyl 4-(3,5-dichloro-4-methylphenyl)-2-methoxy-4-oxobutyrate were added to 4 ml of acetic acid and the mixture was heated to form a solution, to which was then added 0.275 g (0.0055 mole) of hydrazine monohydrate. The mixture was heated under reflux for 3 hours and then cooled, after which it was diluted with 40 ml of water and stirred. The resulting crystals were collected by filtration, washed successively with water and with a small amount of ethyl acetate and then air-dried, to give 1.1 g (yield 86.2%) of the desired 6-(3,5-dichloro-4-methylphenyl)-3(2H)pyridazinone, having properties the same as those of the preceding Examples.

WORKUP

后处理

  1. temperaturethe mixture was heated
  2. customto form a solution
  3. temperatureThe mixture was heated
  4. temperatureunder reflux for 3 hours
  5. temperaturecooled
  6. filtrationThe resulting crystals were collected by filtration
  7. washwashed successively with water and with a small amount of ethyl acetate
  8. customair-dried