HRID1422610

反应详情

EQUATION

反应方程式

HRID 1422610 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Oxalyl chloride (6.8 mL) and N,N-dimethylformamide (0.1 mL) are added to a solution of 3-(2-bromo-3-trifluoromethyl-phenyl)-propionic acid (15.7 g) in dichloromethane (150 mL) at room temperature. The solution is stirred at reflux temperature for 2 h and then concentrated. Trifluoromethane-sulfonic acid (60 ml) is added to the residue, and the resulting mixture is stirred at 55° C. for 4 h. After cooling to room temperature, the mixture is poured into ice-cold water, and the resulting mixture is stirred for 5 min. The precipitate formed is separated by filtration, washed with water, and dissolved in ethyl acetate. The solution is washed with aqueous NaHCO3 solution, dried (Na2SO4), and concentrated. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 90:10→80:20) to afford the title compound. LC (method 4): tR=1.04 min.

WORKUP

后处理

  1. temperatureat reflux temperature for 2 h
  2. concentrationconcentrated
  3. additionTrifluoromethane-sulfonic acid (60 ml) is added to the residue
  4. stirringthe resulting mixture is stirred at 55° C. for 4 h
  5. additionthe mixture is poured into ice-cold water
  6. stirringthe resulting mixture is stirred for 5 min
  7. customThe precipitate formed
  8. customis separated by filtration
  9. washwashed with water
  10. dissolutiondissolved in ethyl acetate
  11. washThe solution is washed with aqueous NaHCO3 solution
  12. dry with materialdried (Na2SO4)
  13. concentrationconcentrated
  14. customThe residue is chromatographed on silica gel (cyclohexane/ethyl acetate 90:10→80:20)