HRID507027

反应详情

EQUATION

反应方程式

HRID 507027 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

Add cesium fluoride (184.3 g, 1.21 mol), methyl boronic acid (63.7 g, 1.05 mol, 3 mol equiv.) and bis(diphenylphosphinoferrocene)palladium(II) chloride (27.83 g, 35.1 mmol) to a solution of methyl 2-amino-5-iodo-4-trifluoromethylbenzoate (121 g, 351 mmol) in anhydrous 1,4-dioxane (2.5 L) at room temperature under an atmosphere of nitrogen and heat the mixture at 80° C. for 3 h. Allow the mixture to cool to room temperature then partition between ethyl acetate (2.5 L) and water (2.5 L) and filter through a pad of Celite® to remove the fine black suspension. Extract the aqueous phase with ethyl acetate (2×100 mL) and wash the combined organic extracts with brine (1 L). Dry over anhydrous magnesium sulfate, filter and remove the solvent under reduced pressure at 45° C. to give a red oil. Purify the residue by column chromatography on silica gel, eluting with isohexane/ethyl acetate (9:1), to give the title compound as a pale yellow crystalline solid (75.25 g, 92%). 1H NMR (300 MHz, CDCl3) δ 7.73 (s, 1H), 6.93 (s, 1H), 5.70 (s, 2H), 3.90 (s, 3H), 2.33 (s, 3H).

WORKUP

后处理

  1. temperatureAllow the mixture to cool to room temperature
  2. customthen partition between ethyl acetate (2.5 L) and water (2.5 L)
  3. filtrationfilter through a pad of Celite®
  4. customto remove the fine black suspension
  5. extractionExtract the aqueous phase with ethyl acetate (2×100 mL)
  6. washwash the combined organic extracts with brine (1 L)
  7. dry with materialDry over anhydrous magnesium sulfate
  8. filtrationfilter
  9. customremove the solvent under reduced pressure at 45° C.
  10. customto give a red oil
  11. customPurify the residue by column chromatography on silica gel
  12. washeluting with isohexane/ethyl acetate (9:1)