HRID632335

反应详情

EQUATION

反应方程式

HRID 632335 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

In a 500 ml two-necked-round-bottom flask, 3-bromo-2-chloro-6-methylpyridine (CAN 185017-72-5) (4.0 g, 19.4 mmol) was suspended in H2O (160 ml) to give a colorless suspension. Under stirring, sodium dodecyl sulfate (64 mg, 222 μmol) and KMnO4 (9.19 g, 58.1 mmol) were added. The reaction mixture was stirred at 100° C. for 18 h. The reaction was then cooled to RT and 100 ml NaHSO3-solution (40%) was added dropwise under ice bath-cooling (decolorization). A white precipitate formed and the mixture was stirred a further 30 min. The reaction mixture was acidified with 120 ml 2N-HCl followed by extraction with ethyl acetate (2×200 ml). The combined organic layer was dried over Na2SO4, filtered off and concentrated in vacuo to give a white solid containing a mixture of starting material and the product. The solid was dissolved in 50 ml TBME/THF 9:1 and under stirring was added 15 ml 2N—NaOH which formed a suspension. The suspension was then extracted with 100 ml water. The water-layer was washed with 50 ml TBME. The water-layer was acidified with 20 ml 2N-HCl which was then extracted with a mixture TBME/THF 9:1 (2×50 ml). The combined organic layers were dried over Na2SO4, filtered off and concentrated in vacuo to dryness to give the title compound (1.8 g, 39%) as a white solid; MS (LC/MS): 235.9[M−H]−.

WORKUP

后处理

  1. customto give a colorless suspension
  2. stirringThe reaction mixture was stirred at 100° C. for 18 h
  3. customA white precipitate formed
  4. stirringthe mixture was stirred a further 30 min
  5. extractionfollowed by extraction with ethyl acetate (2×200 ml)
  6. dry with materialThe combined organic layer was dried over Na2SO4
  7. filtrationfiltered off
  8. concentrationconcentrated in vacuo
  9. customto give a white solid
  10. additioncontaining
  11. additiona mixture of starting material
  12. stirringunder stirring
  13. customformed a suspension
  14. extractionThe suspension was then extracted with 100 ml water
  15. washThe water-layer was washed with 50 ml TBME
  16. extractionwas then extracted with a mixture TBME/THF 9:1 (2×50 ml)
  17. dry with materialThe combined organic layers were dried over Na2SO4
  18. filtrationfiltered off
  19. concentrationconcentrated in vacuo to dryness