HRID718213

反应详情

EQUATION

反应方程式

HRID 718213 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-5 °C

PROCEDURE

实验过程

To a 250 mL of 4-necked flask equipped with an internal thermometer and a condenser was added ethoxybenzene (6.4 g, 52.5 mmol) and dichloromethane (19.2 mL) and the mixture was cooled to −5° C. Aluminum (III) chloride (7.4 g, 55 mmol) was added over 1 h while maintaining the internal temperature below 0° C. After the addition was completed, the mixture was stirred for 30 min at 0˜5° C., and a solution of 2-chloro-5-iodobenzoyl chloride (15.0 g, 50 mmol) in dichloromethane (21 mL) was added dropwise over 1 hour while maintaining the internal temperature below 5° C. The mixture was stirred for another 1 hour at 0˜5° C. and warmed to 10˜15° C. Polymethylhydrosiloxane (PMHS) (15.0 g, 0.25 mol) was added dropwise while maintaining the internal temperature below 25° C. After stirring for 10 hours at 25° C., additional PMHS (9.0 g, 0.15 mol) was added to the above mixture. After stirring for another 16 hours at 30° C., the mixture was cooled to 5˜10° C. and ice water (50 mL) was added slowly dropwise over 1 hour with stirring. The mixture was filtered and the filter cake was slurried with dichloromethane (100 mL) containing diatomite (20 g). The mixture was filtered and the filter cake was washed with dichloromethane (2×50 mL). The combined organic layers were washed with brine (100 mL). After removal of the volatiles, the residue was dissolved in absolute ethanol (45 mL) and refluxed with mechanical stirring (100 RPM) and cooled to 0° C. After stirring for another 16 h at 0˜5° C., the mixture was filtered and the filter cake was washed with pre-cooled (0˜5° C.) ethanol (2×5 mL), dried under vacuum at 40° C. for 12 h to give 14.2 g of 1-chloro-2-(4-ethoxybenzyl)-4-iodobenzene as a white solid. This solid was recrystallized from ethanol (42.6 mL) to give 12.5 g of 1-chloro-2-(4-ethoxybenzyl)-4-iodobenzene as a white solid. Yield, 67%, HPLC purity, HPLC-0002: 99.5%. 1H NMR (CDCl3, 400 MHz): δ 7.21˜7.29 (m, 3H), 7.11 (d, J=8.8 Hz, 2H), 6.85 (d, J=8.8 Hz, 2H), 3.99˜4.07 (m, 4H), 1.43 (t, J=7.2 Hz, 3H).

WORKUP

后处理

  1. customTo a 250 mL of 4-necked flask equipped with an internal thermometer and a condenser
  2. temperaturewhile maintaining the internal temperature below 0° C
  3. additionAfter the addition
  4. temperaturewhile maintaining the internal temperature below 5° C
  5. stirringThe mixture was stirred for another 1 hour at 0˜5° C.
  6. temperaturewarmed to 10˜15° C
  7. temperaturewhile maintaining the internal temperature below 25° C
  8. stirringAfter stirring for 10 hours at 25° C.
  9. stirringAfter stirring for another 16 hours at 30° C.
  10. temperaturethe mixture was cooled to 5˜10° C.
  11. stirringwith stirring
  12. filtrationThe mixture was filtered
  13. additioncontaining diatomite (20 g)
  14. filtrationThe mixture was filtered
  15. washthe filter cake was washed with dichloromethane (2×50 mL)
  16. washThe combined organic layers were washed with brine (100 mL)
  17. customAfter removal of the volatiles
  18. dissolutionthe residue was dissolved in absolute ethanol (45 mL)
  19. temperaturerefluxed
  20. stirringwith mechanical stirring (100 RPM)
  21. temperaturecooled to 0° C
  22. stirringAfter stirring for another 16 h at 0˜5° C.
  23. filtrationthe mixture was filtered
  24. washthe filter cake was washed
  25. temperaturewith pre-cooled (0˜5° C.) ethanol (2×5 mL)
  26. customdried under vacuum at 40° C. for 12 h