HRID2207414

反应详情

EQUATION

反应方程式

HRID 2207414 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

In 2 L flask outfitted with condenser and stir bar was added 1-bromo-3-methyl-5-nitrobenzene (50.0 g, 231 mmol), ethanol (967 mL), and saturated aqueous NH4Cl (141 mL). The system was evacuated and flushed with N2(g) and then iron (38.8 g, 694 mmol) was added before heating the reaction to reflux for 2 days. The reaction was cooled to room temperature and CELITE (15 g) was added to the flask. This was then filtered through CELITE, washing the cake with ethanol (500 mL) and ethyl acetate (500 mL). The filtrate was concentrated and the solvent was removed. The residue was diluted with ethyl acetate (500 mL) and water (500 mL). After cutting the layers, the organic was washed with saturated aqueous NaHCO3 (400 mL) and then brine (400 mL), before drying over sodium sulfate and concentrating. MTBE (˜500 mL) was added to the resultant residue and HCl in dioxane (4 M, 57.9 mL, 231 mmol) was added dropwise at RT over 30 min. The resultant precipitate was collected by filtration. This creme colored solid was placed in a beaker and was dissolved in ethyl acetate and partitioned with saturated aqueous NaHCO3 and then 10% NH4OH (aq). The organic was cut and dried over sodium sulfate before concentrating to dryness. 3-Bromo-5-methylaniline was isolated as a brown oil. MS APCI calc'd for C7H9BrN [M+H]+ 186. found 186/188.

WORKUP

后处理

  1. customIn 2 L flask outfitted with condenser
  2. customThe system was evacuated
  3. customflushed with N2(g)
  4. temperaturebefore heating
  5. customthe reaction
  6. temperatureto reflux for 2 days
  7. additionCELITE (15 g) was added to the flask
  8. filtrationThis was then filtered through CELITE
  9. washwashing the cake with ethanol (500 mL) and ethyl acetate (500 mL)
  10. concentrationThe filtrate was concentrated
  11. customthe solvent was removed
  12. additionThe residue was diluted with ethyl acetate (500 mL) and water (500 mL)
  13. washthe organic was washed with saturated aqueous NaHCO3 (400 mL)
  14. dry with materialbrine (400 mL), before drying over sodium sulfate
  15. concentrationconcentrating
  16. additionwas added dropwise at RT over 30 min
  17. filtrationThe resultant precipitate was collected by filtration
  18. dissolutionwas dissolved in ethyl acetate
  19. custompartitioned with saturated aqueous NaHCO3
  20. dry with materialdried over sodium sulfate
  21. concentrationbefore concentrating to dryness