HRID1452926

反应详情

EQUATION

反应方程式

HRID 1452926 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

5-Fluoro-2-methylsulfonylphenylamine can be obtained in the following way: 1.25 ml of water and 0.47 ml of an aqueous 12N hydrochloric acid solution are added to a solution of 1.2 g of 4-fluoro-1-methylsulfonyl-2-nitrobenzene in 80 ml of ethanol. The reaction mixture is then heated at the reflux of the solvent and 0.92 g of powdered iron are added portionwise. The reaction mixture is then stirred at the reflux of the solvent for 2 hours, then at a temperature in the region of 20° C. for 16 hours. It is then filtered through sintered glass and the solid is washed with ethanol. The filtrate is concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. The residue is taken up in a mixture of water and ethyl acetate and then basified with an aqueous sodium hydrogencarbonate solution, to a pH in the region of 10, and allowed to settle out. The aqueous phase is extracted with 4 times 50 ml of ethyl acetate. The organic extracts are pooled, washed with water, dried over magnesium sulfate, treated with 3S black, filtered and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. 1 g of 5-fluoro-2-methylsulfonylphenylamine is thus obtained in the form of a beige oil which crystallizes (Rf=0.33, silica gel thin layer chromatography, eluent: dichloromethane).

WORKUP

后处理

  1. temperatureThe reaction mixture is then heated at the
  2. additionare added portionwise
  3. temperaturereflux of the solvent for 2 hours
  4. filtrationIt is then filtered through sintered glass
  5. washthe solid is washed with ethanol
  6. concentrationThe filtrate is concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C
  7. additionThe residue is taken up in a mixture of water and ethyl acetate
  8. extractionThe aqueous phase is extracted with 4 times 50 ml of ethyl acetate
  9. washwashed with water
  10. dry with materialdried over magnesium sulfate
  11. additiontreated with 3S black
  12. filtrationfiltered
  13. concentrationconcentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C