HRID1180610

反应详情

EQUATION

反应方程式

HRID 1180610 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

4-Amino-5-iodo-2-trifluoromethyl-benzonitrile (8.04 g, 25.77 mmoles) was dissolved in anhydrous THF (60 mL), stirred under a nitrogen atmosphere and cooled in an ice/brine bath for 20 min. 1.0 M potassium tert-butoxide in THF (82 mL, 82 mmoles) was added and the reaction mixture was stirred for 20 min. Methanesulfonyl chloride (3.2 mL, 41.18 mmoles) was then added and the reaction mixture was stirred at ambient temperature overnight. The reaction mixture was quenched with 1N HCl (90 mL) and extracted with dichloromethane (3×100 mL). The organic extracts were diluted with diethyl ether and a white solid precipitated. The solid was filtered, washed and dried to yield the title compound. The filtrate was concentrated to a crude orange solid. The compound was purified by column chromatography (SiO2, 100% CH2Cl2).

WORKUP

后处理

  1. temperaturecooled in an ice/brine bath for 20 min
  2. stirringthe reaction mixture was stirred for 20 min
  3. stirringthe reaction mixture was stirred at ambient temperature overnight
  4. customThe reaction mixture was quenched with 1N HCl (90 mL)
  5. extractionextracted with dichloromethane (3×100 mL)
  6. additionThe organic extracts were diluted with diethyl ether
  7. customa white solid precipitated
  8. filtrationThe solid was filtered
  9. washwashed
  10. customdried