HRID1084627

反应详情

EQUATION

反应方程式

HRID 1084627 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

2-Nitro-4-chlorobenzoyl chloride (2.2 g, 10 mmol) and 4,4,6,6-tetramethyl-1,3,5-cyclohexanetrione (1.8 g, 10 mmol) were dissolved in methylene chloride. Triethylamine was added and the resulting solution stirred at room temperature for 30 minutes. The solution was washed with 1 normal hydrochloric acid (1N HCl), and saturated sodium chloride (brine), dried over anhydrous magnesium sulfate (MgSO4) and concentrated under vacuum. The residue was dissolved in 20 ml acetonitrile. Triethylamine (5 ml, 3.5 equivalents) and acetone cyanohydrin (0.5 g, 0.6 equivalent) were added and the mixture stirred at room temperature for 4 hours. After dilution with ether, the solution was washed with 1N HCl and extracted with 5% K2CO3. The basic extract was acidified with HCl and extracted with ether. The ether extract was washed with brine, dried over MgSO4 and concentrated under vacuum, yielding 2.2 g of crude product.

WORKUP

后处理

  1. washThe solution was washed with 1 normal hydrochloric acid (1N HCl), and saturated sodium chloride (brine)
  2. dry with materialdried over anhydrous magnesium sulfate (MgSO4)
  3. concentrationconcentrated under vacuum
  4. dissolutionThe residue was dissolved in 20 ml acetonitrile
  5. stirringthe mixture stirred at room temperature for 4 hours
  6. washAfter dilution with ether, the solution was washed with 1N HCl
  7. extractionextracted with 5% K2CO3
  8. extractionThe basic extract
  9. extractionextracted with ether
  10. extractionThe ether extract
  11. washwas washed with brine
  12. dry with materialdried over MgSO4
  13. concentrationconcentrated under vacuum