HRID550601

反应详情

EQUATION

反应方程式

HRID 550601 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a solution of 2-dimethylaminoethanol (6.67 mL, 64.8 mmol) in anhydrous THF (100 mL), at 0° C., potassium tert-butoxide (6.66 g, 59.4 mmol) was added. The mixture was stirred at 0° C. for 1 h, then 4-fluoro-2-nitro-benzoic acid tert-butyl ester (10 g, 41.5 mmol) in anhydrous THF (50 mL) was added dropwise. After 2 hours at 0° C., the mixture was poured into water (1 L) and extracted with ethyl acetate (4×200 mL). The organic phase was washed with water, brine, dried with anhydrous sodium sulfate, filtered and evaporated to dryness. The crude was purified by flash chromatography, using dichloromethane-EtOH-33% NH4OH 9:1:0.01 as eluant, to give the title compound (4.53 g) as yellow oil.

WORKUP

后处理

  1. waitAfter 2 hours at 0° C.
  2. extractionextracted with ethyl acetate (4×200 mL)
  3. washThe organic phase was washed with water, brine
  4. dry with materialdried with anhydrous sodium sulfate
  5. filtrationfiltered
  6. customevaporated to dryness
  7. customThe crude was purified by flash chromatography