HRID275643

反应详情

EQUATION

反应方程式

HRID 275643 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

20 ml of distilled water and 20 ml of 12 N hydrochloric acid are placed, with stirring, in a three-necked flask, and 10 ml of 3-methylthioaniline are then added using a dropping funnel. The mixture is warmed to ensure dissolution and is then cooled down to 5° C. 5.86 g of sodium nitrite dissolved in 15 ml of water are subsequently added slowly, using a dropping funnel, while maintaining the temperature between 5 and 8° C. 20 min after having completed the addition, 13.57 g of potassium iodide dissolved in 15 ml of water are added over a period of 10 min and the mixture is then stirred at room temperature for 15 h. The oil which forms is separated from the aqueous phase by decantation, and an aqueous solution of sodium thiosulphate is then added to it. The aqueous phase is decanted and the product is extracted with 100 ml of dichloromethane. The organic phase is washed with 100 ml of water, and the aqueous phase is adjusted to pH 9 with concentrated sodium hydroxide solution, and then separated off. The organic phase is washed with 2 times 100 ml of water, separated off, dried over magnesium sulphate, filtered and then concentrated to dryness under reduced pressure (50 kPa) at 40° C. The resulting product is purified by flash chromatography (eluent, cyclohexane) in order to yield 13 g of 3-iodo-1-methylthiobenzene in the form of a yellow liquid (Merck Silica 5719, Rf=0.8/cyclohexane).

WORKUP

后处理

  1. temperatureThe mixture is warmed
  2. dissolutiondissolution
  3. additionare subsequently added slowly
  4. temperaturewhile maintaining the temperature between 5 and 8° C
  5. custom20 min
  6. additionare added over a period of 10 min
  7. stirringthe mixture is then stirred at room temperature for 15 h
  8. customThe oil which forms is separated from the aqueous phase by decantation
  9. additionan aqueous solution of sodium thiosulphate is then added to it
  10. customThe aqueous phase is decanted
  11. extractionthe product is extracted with 100 ml of dichloromethane
  12. washThe organic phase is washed with 100 ml of water
  13. customseparated off
  14. washThe organic phase is washed with 2 times 100 ml of water
  15. customseparated off
  16. dry with materialdried over magnesium sulphate
  17. filtrationfiltered
  18. concentrationconcentrated to dryness under reduced pressure (50 kPa) at 40° C
  19. customThe resulting product is purified by flash chromatography (eluent, cyclohexane) in order