HRID533518

反应详情

EQUATION

反应方程式

HRID 533518 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

4-Bromo-2-fluoro-phenyl-acetic acid (36 g, 154 mmol) (40.6 g, 174 mmol) was dissolved in THF (100 mL), and cooled to 0° C. in an ice-bath. Borane (1 M in THF, 200 mL, 1.2 eq) was then added dropwise. During the addition, the temperature rose slowly to 27° C. After complete addition the ice-bath was removed and the reaction mixture was stirred for 1 hour at room temperature. The reaction mixture was added carefully to saturated aqueous K2CO3 (300 mL), and the obtained suspension was diluted with H2O (500 mL). The THF layer was separated and concentrated under reduced pressure. The aqueous layer was extracted with EtOAc (2×100 mL). The residue from the concentrated THF layer was dissolved into the combined organic layers, which was washed with brine. The organic layer was dried (Na2SO4), filtered, and concentrated under reduced pressure, yielding crude material (35.6 g) as a yellow oil, which solidified to a white solid upon standing. The crude material was purified by column chromatography (SiO2; 1750 mL, 0-5% MeOH in CH2Cl2), yielding the title compound as a white solid (31.5 g, 144 mmol, 82%). 1H-NMR (CDCl3, 300 MHz): 1.50 (s, 1H); 2.95 (t, 2H); 3.92 (t, 2H); 7.18 (t, 1H); 7.28 (m, 1H)

WORKUP

后处理

  1. additionDuring the addition
  2. customrose slowly to 27° C
  3. customwas removed
  4. additionThe reaction mixture was added carefully to saturated aqueous K2CO3 (300 mL)
  5. additionthe obtained suspension was diluted with H2O (500 mL)
  6. customThe THF layer was separated
  7. concentrationconcentrated under reduced pressure
  8. extractionThe aqueous layer was extracted with EtOAc (2×100 mL)
  9. dissolutionThe residue from the concentrated THF layer was dissolved into the combined organic layers, which
  10. washwas washed with brine
  11. dry with materialThe organic layer was dried (Na2SO4)
  12. filtrationfiltered
  13. concentrationconcentrated under reduced pressure
  14. customyielding crude material (35.6 g) as a yellow oil, which
  15. customThe crude material was purified by column chromatography (SiO2; 1750 mL, 0-5% MeOH in CH2Cl2)