HRID129600

反应详情

EQUATION

反应方程式

HRID 129600 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of methyl 2-(3-aminophenoxy)phenylacetate (11.54 g) and methyl formate (27.7 ml) in DMF (25 ml) was added dropwise to a stirred suspension of sodium hydride (3.25 g) in DMF (50 ml) cooled in ice to below 10° C. (effervescence). Following the addition, the reaction mixture was stirred at room temperature for 3 hours, poured into water, acidified with concentrated hydrochloric acid and extracted with ethyl acetate. These extracts were washed with brine, dried and concentrated to give a viscous yellow oil. Potassium carbonate (12.4 g) and dimethyl sulphate (4.25 ml) were added successively to a stirred solution of this yellow oil in DMF (50 mls) and the resulting mixture was stirred at room temperature for 3 hours, poured into water and extracted with ethyl acetate. The extracts were washed with water, dried and concentrated to give (E)-methyl 2-[2-(3-formamidophenoxy)phenyl]-3-methoxypropenoate (13.67, 93% yield) as a clear green gum.

WORKUP

后处理

  1. temperaturecooled in ice to below 10° C. (effervescence)
  2. additionthe addition
  3. extractionextracted with ethyl acetate
  4. washThese extracts were washed with brine
  5. customdried
  6. concentrationconcentrated
  7. customto give a viscous yellow oil
  8. stirringthe resulting mixture was stirred at room temperature for 3 hours
  9. extractionextracted with ethyl acetate
  10. washThe extracts were washed with water
  11. customdried
  12. concentrationconcentrated