HRID2395346

反应详情

EQUATION

反应方程式

HRID 2395346 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

4-Nitrophenol(41 mmoles, 5.1 g) was dissolved in DMF (500 ml) and treated with sodium hydride (41 mmoles previously washed with hexane). After stirring at room temperature for 1 hr, 2-chloroquinoline (40 mmoles, 6.5 g) was added dropwise and stirred for 16 hr at room temperature followed by refluxing for 6 hr. Water was added to the cooled solution and the product was extracted with ethyl acetate. The ethyl acetate solution was washed with water, and 5N NaOH, dried over sodium sulfate and concentrated. The product was purified by HPLC over silica gel eluted with ethyl acetate/hexane to yield 2-(4-nitrophenoxy)quinoline. 3.1 mmoles, 8%. Mass Spec (FD) 266. Calcd for C15H10N2O3 : C 67.45; H, 3.84; N, 10.40. Found: C, 65.84; H, 3.88; N, 8.47.

WORKUP

后处理

  1. washpreviously washed with hexane)
  2. stirringstirred for 16 hr at room temperature
  3. temperatureby refluxing for 6 hr
  4. extractionthe product was extracted with ethyl acetate
  5. washThe ethyl acetate solution was washed with water, and 5N NaOH
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated
  8. customThe product was purified by HPLC over silica gel
  9. washeluted with ethyl acetate/hexane