HRID628777

反应详情

EQUATION

反应方程式

HRID 628777 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
120 °C

PROCEDURE

实验过程

In a stirred nitrogen covered reactor N-methyl-pyrrolidone, NMP (4.5 L) was flushed with nitrogen for 20 minutes. 4-Methylbenzenethiol (900 g, 7.25 mol) was added and then 1,2-dibromobenzene (1709 g, 7.25 mol). Potassium tert-butoxide (813 g, 7.25 mol) was finally added as the last reactant. The reaction was exothermic giving a temperature rise of the reaction mixture to 70° C. The reaction mixture was then heated to 120° C. for 2-3 hours. The reaction mixture was cooled to room temperature. Ethyl acetate (4 L) was added and aqueous sodium chloride solution (15%, 2.5 L). The mixture was stirred for 20 minutes. The aqueous phase was separated and extracted with another portion of ethyl acetate (2 L). The aqueous phase was separated and the organic phases were combined and washed with sodium chloride solution (15%, 2.5 L) The organic phase was separated, dried with sodium sulphate and evaporated at reduced pressure to a red oil which contains 20-30% NMP. The oil was diluted to twice the volume with methanol and the mixture was refluxed. More methanol was added until a clear red solution was obtained. The solution was cooled slowly to room temperature while seeded. The product crystallises as off white crystals, they were isolated by filtration and washed with methanol and dried at 40° C. in a vacuum oven until constant weight.

WORKUP

后处理

  1. customIn a stirred nitrogen covered reactor N-methyl-pyrrolidone, NMP (4.5 L) was flushed with nitrogen for 20 minutes
  2. customThe reaction was exothermic giving a temperature rise of the reaction mixture to 70° C
  3. temperatureThe reaction mixture was cooled to room temperature
  4. customThe aqueous phase was separated
  5. extractionextracted with another portion of ethyl acetate (2 L)
  6. customThe aqueous phase was separated
  7. washwashed with sodium chloride solution (15%, 2.5 L) The organic phase
  8. customwas separated
  9. dry with materialdried with sodium sulphate
  10. customevaporated at reduced pressure to a red oil which
  11. additionThe oil was diluted to twice the volume with methanol
  12. temperaturethe mixture was refluxed
  13. additionMore methanol was added until a clear red solution
  14. customwas obtained
  15. temperatureThe solution was cooled slowly to room temperature
  16. customThe product crystallises as off white crystals
  17. customthey were isolated by filtration
  18. washwashed with methanol
  19. customdried at 40° C. in a vacuum oven until constant weight