HRID1110882

反应详情

EQUATION

反应方程式

HRID 1110882 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Oxalyl chloride (9.62 ml, 0.11 mole) was dissolved in 45 ml CH2Cl2. A solution of di-(4-fluorophenyl)amine (19.7 g, 0.096 mole) in 145 ml CH2Cl2 was added over 15 minutes; the temperature rose from 23° to 28°. After stirring 1 hour, AlCl3 (40.8 g) was added portionwise over 15 minutes; the temperature rose from 20° to 30°, and was kept less than 30° by cooling.. After stirring for 10 minutes, the reaction mixture was added to 250 ml ethyl acetate and 500 ml ice and water (the temperature rose to 30° C.). The aqueous layer was washed 2×250 ml ethyl acetate The organic layers were combined, back-washed 1×400 ml H2O, dried over MgSO4, evaporated to solids and triturated with 100 ml 1:1 ether:hexane to recover title product, 19.9 g, m.p. 180°-190°, tlc Rf 0.55 (1:1 ether;hexane)

WORKUP

后处理

  1. customrose from 23° to 28°
  2. customrose from 20° to 30°
  3. customwas kept less than 30°
  4. temperatureby cooling
  5. stirringAfter stirring for 10 minutes
  6. customrose to 30° C.
  7. washThe aqueous layer was washed 2×250 ml ethyl acetate The organic layers
  8. washback-washed 1×400 ml H2O
  9. dry with materialdried over MgSO4
  10. customevaporated to solids
  11. customtriturated with 100 ml 1:1 ether
  12. customhexane to recover title product, 19.9 g, m.p. 180°-190°, tlc Rf 0.55 (1:1 ether;hexane)