HRID351664

反应详情

EQUATION

反应方程式

HRID 351664 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a suspension of 5-tert-butyl-2-methoxy-1,3-dinitrobenzene (10.2 g, 0.04 mol) in EtOAc (150 mL) was added in a single portion a solution of sodium sulfide nonahydrate (19.2 g, 0.08 mol) in water (200 mL). Aliquate® 336 (0.8 g, 5 mole %) was added in a single portion, and the two-phase mixture was brought to a reflux. All solids dissolved, and the mixture became red/brown. After about 3 h, TLC (3:1 hexanes:EtOAc) revealed almost complete loss of starting material. The mixture was filtered warm through a pad of diatomaceous earth to remove insolubles, and the filter cake was washed with fresh EtOAc. The clarified two-phase mixture was separated, and the organic layer was washed with sodium carbonate solution, followed by water and then saturated sodium chloride solution. After drying over magnesium sulfate, the solution was concentrated under reduced pressure to a thick, dark oil. This oil was extracted three times with refluxing hexanes, leaving behind a dark residue. The orange extract deposited some more dark oil, from which the warm supernatant was decanted. The resulting orange solution was heated back to reflux, and treated with both activated charcoal and diatomaceous earth. The solution was filtered hot, and the filter cake washed with hot hexanes. Re-heating the orange filtrate resulted in a clear solution. Quickly cooling the solution in an ice/acetone bath and scratching the flask with a glass rod resulted in the deposition of an orange/yellow precipitate. The suspension was allowed to cool for 1 h, and then filtered. The filter cake was washed with a small portion of cold hexanes, and then dried on the filter, providing the title compound as a yellow/orange powder (2.6 g, 30%).

WORKUP

后处理

  1. additionAliquate® 336 (0.8 g, 5 mole %) was added in a single portion
  2. dissolutionAll solids dissolved
  3. filtrationThe mixture was filtered
  4. temperaturewarm through a pad of diatomaceous earth
  5. customto remove insolubles
  6. washthe filter cake was washed with fresh EtOAc
  7. customThe clarified two-phase mixture was separated
  8. washthe organic layer was washed with sodium carbonate solution
  9. dry with materialAfter drying over magnesium sulfate
  10. concentrationthe solution was concentrated under reduced pressure to a thick, dark oil
  11. extractionThis oil was extracted three times with refluxing hexanes
  12. customleaving behind a dark residue
  13. extractionThe orange extract
  14. customfrom which the warm supernatant was decanted
  15. temperatureThe resulting orange solution was heated back
  16. temperatureto reflux
  17. additiontreated with both activated charcoal and diatomaceous earth
  18. filtrationThe solution was filtered hot
  19. washthe filter cake washed with hot hexanes
  20. customRe-heating the orange filtrate resulted in a clear solution
  21. temperatureQuickly cooling the solution in an ice/acetone bath
  22. customresulted in the deposition of an orange/yellow precipitate
  23. temperatureto cool for 1 h
  24. filtrationfiltered
  25. washThe filter cake was washed with a small portion of cold hexanes
  26. customdried on the filter