HRID384382

反应详情

EQUATION

反应方程式

HRID 384382 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

Di-tert-butyl 1-(2,2-dimethyl-1H-inden-5-yl)hydrazine-1,2-dicarboxylate 45c (3.3 g, 8.78 mmol) was dissolved in 12 mL of acetic acid followed by addition of 6 mL of trifluoroacetic acid and 3-oxo-butanoic acid methyl ester (1.5 mL, 13.8 mmol). Upon completion of the addition, the reaction mixture was stirred at 90° C. for 2 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was concentrated under reduced pressure and the residue was diluted with 30 mL of water and 30 mL of ethyl acetate. After mixing well, the separated organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, filtered to remove the drying agent and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 2-(2,2-dimethyl-indan-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one 45d (464 mg, yield 22.1%) as a yellow oil.

WORKUP

后处理

  1. additionUpon completion of the addition
  2. concentrationThe mixture was concentrated under reduced pressure
  3. additionthe residue was diluted with 30 mL of water and 30 mL of ethyl acetate
  4. additionAfter mixing well
  5. washthe separated organic layer was washed with saturated brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. customto remove the drying agent
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by silica gel column chromatography