HRID579259

反应详情

EQUATION

反应方程式

HRID 579259 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
33 °C

PROCEDURE

实验过程

To a 2 L volume four-necked flask, magnesium (cutting chip) (66.2 g), tetrahydrofuran (anhydrous) (494 g), and toluene (549 g) were added under a nitrogen atmosphere at room temperature. After starting to stir the mixture, dibromoethane (26.9 g) was added dropwise over 10 minutes at about 20° C., and then the internal temperature was raised to 33° C. The resulting mixture was stirred at 30° C. for 20 minutes. 2,6-diethyl-4-methylbromobenzene (10-a) (549.0 g) was added dropwise thereto at 40° C. over 1 hour. The resulting mixture was stirred at 50° C. for 51 hours, and diethyl oxalate (389.1 g) dissolved in toluene (550.1 g) was added dropwise thereto at about 0° C. over 1 hour. The resulting mixture was stirred at about 5° C. for 1 hour. Then, to the mixture, 3.5 w/w % of hydrochloric acid (832 g) was added dropwise at the same temperature. Then the mixture was warmed to room temperature, and the organic layer was separated. The aqueous layer was extracted with toluene (548.3 g). The organic layers were combined, washed with water (1098 g) and concentrated under reduced pressure to give 710.8 g of ethyl 2-(2,6-diethyl-4-methylphenyl)-2-oxoacetate (9-a).

WORKUP

后处理

  1. additionwas added dropwise over 10 minutes at about 20° C.
  2. waitat 40° C. over 1 hour
  3. stirringThe resulting mixture was stirred at 50° C. for 51 hours
  4. additionwas added dropwise
  5. waitat about 0° C. over 1 hour
  6. stirringThe resulting mixture was stirred at about 5° C. for 1 hour
  7. additionwas added dropwise at the same temperature
  8. temperatureThen the mixture was warmed to room temperature
  9. customthe organic layer was separated
  10. extractionThe aqueous layer was extracted with toluene (548.3 g)
  11. washwashed with water (1098 g)
  12. concentrationconcentrated under reduced pressure