HRID225751

反应详情

EQUATION

反应方程式

HRID 225751 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

23.2 g (180.5 mM) of 5-amino-2-chloropyridine are mixed in 70 ml of dichloro-methane (DCM) and 180 ml of methanol, and 21.6 g (216 mM) of calcium carbonate and 75.3 g (226 mM) of benzyltrimethylammonium dichloroiodate are added. The reaction mixture is stirred at room temperature for 16 hours, and then filtered to remove the mineral salts. The filtrate is diluted with water and extracted with DCM. The organic phase obtained is washed with sodium chloride solution, and then with saturated sodium thiosulfate solution, dried over magnesium sulfate and concentrated under reduced pressure. An oil is obtained, which is purified by chromatography on silica gel, eluting with a cyclohexane/ethyl acetate mixture (80/20 and then 70/30; v/v). 13.9 g of the expected product are thus obtained in the form of an orange-colored solid (yield=30%).

WORKUP

后处理

  1. filtrationfiltered
  2. customto remove the mineral salts
  3. additionThe filtrate is diluted with water
  4. extractionextracted with DCM
  5. customThe organic phase obtained
  6. washis washed with sodium chloride solution
  7. dry with materialwith saturated sodium thiosulfate solution, dried over magnesium sulfate
  8. concentrationconcentrated under reduced pressure
  9. customAn oil is obtained
  10. customwhich is purified by chromatography on silica gel
  11. washeluting with a cyclohexane/ethyl acetate mixture (80/20