HRID990557

反应详情

EQUATION

反应方程式

HRID 990557 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

The 3-(2,2,2-trifluoroethoxy)benzaldehyde (0.360 g, 1.76 mmol) product from EX-659A and 3-phenoxyaniline (0.326 g, 1.76 mmol) were combined in 50 mL of cyclohexane with 3 Å molecular sieves (1 g) and stirred overnight at 80° C. The mixture was cooled, filtered, and evaporated, then dissolved in 50 mL of methanol and cooled to 0° C. Solid sodium borohydride (0.030 g, 0.79 mmol) was added in portions, and the mixture was stirred overnight. The reaction was quenched with 5% aq. NaHCO3 and extracted with ether (3×). The combined ether layers were washed with water and brine, dried over MgSO4, filtered, and evaporated to give 0.50 g (76%) of the desired N-(3-phenoxyphenyl)[[3-(2,2,2-trifluoroethoxy)phenyl]methyl]amine product as an amber oil, >95% pure by normal phase HPLC analysis. MS m/z=373 [M+].

WORKUP

后处理

  1. temperatureThe mixture was cooled
  2. filtrationfiltered
  3. customevaporated
  4. dissolutiondissolved in 50 mL of methanol
  5. temperaturecooled to 0° C
  6. stirringthe mixture was stirred overnight
  7. customThe reaction was quenched with 5% aq. NaHCO3
  8. extractionextracted with ether (3×)
  9. washThe combined ether layers were washed with water and brine
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. customevaporated