HRID513854

反应详情

EQUATION

反应方程式

HRID 513854 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
150 °C

PROCEDURE

实验过程

N-Benzhydrylidene-N′-(3,5-di-tert-butyl-phenyl)-hydrazine (617 mg, 1.6 mmol) was dissolved in ethanol (12 ml). Then, ethyl pyruvate (212 μl, 1.9 mmol) and p-toluene sulfonic acid monohydrate (914 mg, 4.8 mmol) were added thereto. This was heated and stirred at 150° C. by microwave under a nitrogen atmosphere for one hour. After cooling it to room temperature, the reaction mixture was combined with water and an aqueous solution saturated with sodium bicarbonate. The product was extracted into ethyl acetate. The organic layer was isolated, and washed with an aqueous solution saturated with sodium chloride, and dried over magnesium sulfate. The desiccant was removed by filtration, and concentration was performed. Then, the residue obtained by concentration under reduced pressure was purified by silica gel column chromatography (hexane/ethyl acetate=100/5). Thus, 4,6-di-tert-butyl-1H-indole-2-carboxylic acid ethyl ester was obtained as a brown solid (268 mg, 56%).

WORKUP

后处理

  1. temperatureThis was heated
  2. temperatureAfter cooling it to room temperature
  3. extractionThe product was extracted into ethyl acetate
  4. customThe organic layer was isolated
  5. washwashed with an aqueous solution saturated with sodium chloride
  6. dry with materialdried over magnesium sulfate
  7. customThe desiccant was removed by filtration, and concentration
  8. customThen, the residue obtained by concentration under reduced pressure
  9. customwas purified by silica gel column chromatography (hexane/ethyl acetate=100/5)