HRID584725

反应详情

EQUATION

反应方程式

HRID 584725 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of 2,2,2-trifluoro-N′-(4-methoxyphenyl)ethanehydrazonamide (0.92 g, 3.95 mmol) in 10 mL of dioxane, were added pyridine (0.319 mL, 3.95 mmol) and a solution of 4-methoxybenzoyl chloride (673 mg, 3.95 mmol) in 3 mL of dioxane. The mixture was refluxed with stirring for 12 hours. The solvent was removed under reduced pressure. 50 mL of dichloromethane and 20 mL of 0.1 N hydrochloric acid were added to the residue and the organic layer was separated. The aqueous layer was extracted with 50 mL of dichloromethane. A combined organic layer was washed with 0.1 N hydrochloric acid and brine and dried over magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (toluene-ethyl acetate 9:1) and then recrystallized with diisopropyl ether-hexane to give pale brown needle of 1,5-bis(4-methoxyphenyl)-3-(trifluoromethyl)-1H-1,2,4-triazole (0.67 g, 48.6% yield).

WORKUP

后处理

  1. temperatureThe mixture was refluxed
  2. customThe solvent was removed under reduced pressure
  3. addition50 mL of dichloromethane and 20 mL of 0.1 N hydrochloric acid were added to the residue
  4. customthe organic layer was separated
  5. extractionThe aqueous layer was extracted with 50 mL of dichloromethane
  6. washA combined organic layer was washed with 0.1 N hydrochloric acid and brine
  7. dry with materialdried over magnesium sulfate
  8. customThe solvent was removed under reduced pressure
  9. customThe residue was purified by silica gel column chromatography (toluene-ethyl acetate 9:1)
  10. customrecrystallized with diisopropyl ether-hexane