HRID1060580

反应详情

EQUATION

反应方程式

HRID 1060580 的结构方程式

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

Formaldehyde 48% v/v (65 ml, 0.86 moles) under stirring, then 3-methoxy-benzoic acid (100 g, 0.66 moles) were added to concentrated HCl (1 l) and the mixture was heated at 100° C. by checking the development of gas for 30 minutes. The cooling of the mixture brought to the formation of a precipitate which was filtered and put aside, while the mixture was washed with water, then with 5% NaOH. The new precipitate was extracted twice with CH2Cl2, the extract was anhydrified, concentrated, joined to the previously filtered solid, and both were dissolved in CH2Cl2 and treated with diethylamine (120 ml, 1.15 moles). After 24 hours it was extracted with 10% HCl and the phases were separated with CH2Cl2. The organic phase was washed with 10% NaOH, decoloured with charcoal, anhydrified and concentrated. The residue was dissolved in CH2Cl2 and treated, under stirring, with 10% HCl for 30 minutes. The organic phase was washed with water, anhydrified and concentrated. The residue was dissolved in CH2Cl2 and treated with 10% NaOH under stirring for 30 minutes. The organic phase was washed with water, dried and concentrated to give a solid which was crystallised from aqueous CH3OH. The filtrate was dried at 50° C. on P2O5, then crystallised again from aqueous CH3OH to give 35.28 g of the title compound (yield: 32%).

WORKUP

后处理

  1. customfor 30 minutes
  2. temperatureThe cooling of the mixture
  3. filtrationwas filtered
  4. washwas washed with water
  5. extractionThe new precipitate was extracted twice with CH2Cl2
  6. concentrationconcentrated
  7. dissolutionboth were dissolved in CH2Cl2
  8. extractionAfter 24 hours it was extracted with 10% HCl
  9. customthe phases were separated with CH2Cl2
  10. washThe organic phase was washed with 10% NaOH
  11. concentrationconcentrated
  12. dissolutionThe residue was dissolved in CH2Cl2
  13. additiontreated
  14. washThe organic phase was washed with water, anhydrified
  15. concentrationconcentrated
  16. dissolutionThe residue was dissolved in CH2Cl2
  17. additiontreated with 10% NaOH
  18. stirringunder stirring for 30 minutes
  19. washThe organic phase was washed with water
  20. customdried
  21. concentrationconcentrated
  22. customto give a solid which
  23. customwas crystallised from aqueous CH3OH
  24. customThe filtrate was dried at 50° C. on P2O5
  25. customcrystallised again from aqueous CH3OH