HRID130684

反应详情

EQUATION

反应方程式

HRID 130684 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
-70 °C

PROCEDURE

实验过程

Add n-butyllithium (21.7 mL, 34.8 mmol, 1.6 M in hexanes) to a −70° C. solution of diisopropylamine (4.9 mL, 34.8 mmol) in THF (75 mL). Allow the solution to cool back to −70° C., and add 2-bromopyridine (5.0 g, 31.6 mmol) to the solution while maintaining the temperature below −65° C. Rinse contents of vessel that contained 2-bromopyridine with THF (10 mL) and add this solution to the reaction mixture. Stir the resulting solution for 15 min, and then add a solution of 2-chlorobenzaldehyde (3.55 mL, 31.6 mmol) in THF (15 mL) in a single portion. Stir the resulting solution for approximately 5 h at −70° C. Add MeOH (3.0 mL) and remove cooling. Add 3 N HCl (30 mL) to the reaction mixture followed by toluene (25 mL). Separate the layers, and wash the organic layer with H2O (25 mL). Concentrate the organic layer to approximately 2 total volumes. Add toluene (50 mL) and concentrate the solution to approximately 2 total volumes. Add toluene (65 mL) again, and concentrate the solution to approximately 2 total volumes. Add DMSO (18 mL). Add N,N-diisopropylethylamine (14.5 mL, 83.1 mmol) to the resulting solution. In a separate reaction vessel, dissolve sulfur trioxide pyridine complex (11.6 g, 72.7 mmol) in DMSO (50 mL). Add a portion of the sulfur trioxide pyridine complex/DMSO solution (35 mL) to the reaction mixture and stir for 30 min. Add a second portion of the sulfur trioxide pyridine complex/DMSO solution (9 mL) to the reaction mixture and stir for 30 min. Add a third portion of the sulfur trioxide pyridine complex/DMSO solution (9 mL) and stir for 30 min. Add a final portion of the sulfur trioxide pyridine complex/DMSO solution (approximately 9 mL) and stir for 30 min. Add ethyl acetate (50 mL) and 1 N HCl (100 mL). Separate the layers and extract the aqueous layer with ethyl acetate (25 mL). Separate the layers and extract the combined organic layers with H2O (25 mL). Separate the layers and concentrate the organic layer to approximately 2 total volumes. Add isopropanol (50 mL) and concentrate the resulting solution to approximately 2 total volumes. Add isopropanol (50 mL) and concentrate the resulting solution to approximately 2 total volumes. Add isopropanol (5 mL), and then add heptane (40 mL) dropwise. Stir the resulting slurry for 15 min. Cool the slurry to 0° C. and stir for 1 h. Filter the slurry, rinse the filter cake with chilled heptane (20 mL), and dry to afford the title compound as an off-white solid: 1H NMR (500 MHz, CDCl3) δ 8.49 (dd, J=4.9, 2.0 Hz, 1H), 7.78 (dd, J=7.3, 2.0 Hz, 1H), 7.59 (dd, J=7.3, 1.5 Hz, 1H), 7.49-7.36 (m, 4H); 13C NMR (125 MHz, CDCl3) δ 193.8, 152.0, 139.5, 139.1, 137.7, 136.7, 133.6, 133.3, 131.8, 131.2, 127.4, 123.0. LRMS (ES+) calcd for C12H8BrClNO (M+H+) 295.9, found 295.8 m/z.

WORKUP

后处理

  1. temperaturewhile maintaining the temperature below −65° C
  2. customRinse contents of vessel that contained
  3. stirringStir the resulting solution for approximately 5 h at −70° C
  4. customAdd MeOH (3.0 mL) and remove
  5. temperaturecooling
  6. additionAdd 3 N HCl (30 mL) to the reaction mixture
  7. customSeparate the layers
  8. washwash the organic layer with H2O (25 mL)
  9. concentrationConcentrate the organic layer to approximately 2 total volumes
  10. concentrationAdd toluene (50 mL) and concentrate the solution to approximately 2 total volumes
  11. concentrationAdd toluene (65 mL) again, and concentrate the solution to approximately 2 total volumes
  12. customIn a separate reaction vessel
  13. stirringstir for 30 min
  14. stirringstir for 30 min
  15. stirringstir for 30 min
  16. stirringstir for 30 min
  17. customSeparate the layers
  18. extractionextract the aqueous layer with ethyl acetate (25 mL)
  19. customSeparate the layers
  20. extractionextract the combined organic layers with H2O (25 mL)
  21. customSeparate the layers
  22. concentrationconcentrate the organic layer to approximately 2 total volumes
  23. concentrationAdd isopropanol (50 mL) and concentrate the resulting solution to approximately 2 total volumes
  24. concentrationAdd isopropanol (50 mL) and concentrate the resulting solution to approximately 2 total volumes
  25. stirringStir the resulting slurry for 15 min
  26. temperatureCool the slurry to 0° C.
  27. stirringstir for 1 h
  28. filtrationFilter the slurry
  29. washrinse the filter cake with chilled heptane (20 mL)
  30. customdry