HRID72251

反应详情

EQUATION

反应方程式

HRID 72251 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

4′-Chloro-4-ethyl-3-nitrobiphenyl (22.6 g, 0.086 mol) is suspended in methanol (250 ml) and the reaction mixture is stirred at room temperature. Distilled water (100 ml) is added, followed by zinc dust (39.0 g, 0.60 mol) and ammonium chloride (13.8 g, 0.26 mol) and the mixture is heated to reflux for 1 hour. The reaction mixture is cooled to room temperature, filtered through diatomaceous earth and the filtrate is evaporated in vacuo to remove most of the methanol. The residue is partitioned between ethyl acetate (200 ml) and water and the aqueous phase is re-extracted with ethyl acetate (200 ml). The organic extracts are combined, washed with water and brine, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated in vacuo to give 3-amino-4′-chloro-4-ethylbiphenyl (15.0 g) as a colourless solid. The product is used directly without further purification in Step 5.

WORKUP

后处理

  1. temperaturethe mixture is heated
  2. temperatureto reflux for 1 hour
  3. temperatureThe reaction mixture is cooled to room temperature
  4. filtrationfiltered through diatomaceous earth
  5. customthe filtrate is evaporated in vacuo
  6. customto remove most of the methanol
  7. customThe residue is partitioned between ethyl acetate (200 ml) and water
  8. extractionthe aqueous phase is re-extracted with ethyl acetate (200 ml)
  9. washwashed with water and brine
  10. dry with materialdried over anhydrous magnesium sulfate
  11. filtrationfiltered
  12. customthe filtrate is evaporated in vacuo