HRID1743986

反应详情

EQUATION

反应方程式

HRID 1743986 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
20 °C

PROCEDURE

实验过程

To a clean a dry nitrogen purged acetone boiled out 100 gallon glass lined reactor was charged, 7.9 Kg of N-[(2,5-Difluoro-phenyl)-(toluene-4-sulfonyl)-methyl]-formamide (24, moles), 16 gallons of tetrahydrofuran and 7.8 Kg of phosphorous oxychloride (51 moles). The batch was allowed to stir at 20° C. for 30 minutes and then cooled to 3.5° C. To the batch was added 15.8 Kg of 2,6-lutidine (146 moles) over 15 minutes. The reaction mixture was allowed to warm to 23° C. and was stirred for 17 hours at 23° C. The reaction was judged complete by HPLC and was charged to a 40 gallon solution of 10% sodium bicarbonate at 22° C., and the contents were allowed to stir for 30 minutes. To the batch was then added 25 gallons of ethyl acetate and the layers were separated. The water layer was backwashed with 9 gallons of ethyl acetate and the product rich ethyl acetate combined with the first wash. The product rich ethyl acetate layers were added to a 10% citric acid solution (20 gallons) and then stirred. The organic layer was checked by HPLC for 2,6 lutidine and then separated. The organic layer was washed with 10 gallons of saturated NaCl and dried over 7.9 Kg of magnesium sulfate. The drying agents were removed by filtration and the cake was washed with 4 gallons of ethyl acetate. The ethyl acetate layer was concentrated to 7 gallons under vacuum at an internal temperature of 24° C. The batch was then added to 11 gallons of IPO at 21° C. and allowed to granulate at 4° C. for 12 hours. The product was isolated via filtration and washed with 4 gallons of 5° C. IPO. The product was then dried at 34° C. for 22 hours with nitrogen bleed to recover 5.0 Kg of the title compound (66% yield).

WORKUP

后处理

  1. customTo a clean a dry nitrogen purged acetone
  2. additionwas charged
  3. temperaturecooled to 3.5° C
  4. temperatureto warm to 23° C.
  5. stirringwas stirred for 17 hours at 23° C
  6. stirringto stir for 30 minutes
  7. customthe layers were separated
  8. additionThe product rich ethyl acetate layers were added to a 10% citric acid solution (20 gallons)
  9. stirringstirred
  10. customseparated
  11. washThe organic layer was washed with 10 gallons of saturated NaCl
  12. dry with materialdried over 7.9 Kg of magnesium sulfate
  13. customThe drying agents were removed by filtration
  14. washthe cake was washed with 4 gallons of ethyl acetate
  15. concentrationThe ethyl acetate layer was concentrated to 7 gallons under vacuum at an internal temperature of 24° C
  16. additionThe batch was then added to 11 gallons of IPO at 21° C.
  17. waitto granulate at 4° C. for 12 hours
  18. customThe product was isolated via filtration
  19. washwashed with 4 gallons of 5° C
  20. customThe product was then dried at 34° C. for 22 hours with nitrogen