HRID557159

反应详情

EQUATION

反应方程式

HRID 557159 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Add magnesium chloride (27.7 g, 0.29 mol) to 2-methoxyethanol (400 mL) and heat the mixture to reflux. Add a solution of 3-(3,4-Dihydro-2H-quinolin-1-yl)-2-oxopropionic acid ethyl ester (0.29 mol) in 2-methoxyethanol (100 mL) and tetrahydrofuran (40 mL) slowly to the MgCl2 mixture over 1 hour. Upon completion of addition, stir the mixture for 5 hours at reflux, and then concentrate under reduced pressure. Treat the concentrated crude mixture with 2N hydrochloric acid (500 mL) and extract with dichloromethane (3×400 mL). Combine the organic layers, dry over sodium sulfate, filter, and concentrate under reduced pressure. Subject the residue to silica gel chromatography, eluting with 20% ethyl acetate/hexanes. Combine fractions containing product and concentrate them under reduced pressure to provide the desired compound as an orange solid (31.6 g, 48%).

WORKUP

后处理

  1. temperatureheat the mixture
  2. temperatureto reflux
  3. additionUpon completion of addition
  4. temperatureat reflux
  5. concentrationconcentrate under reduced pressure
  6. additionTreat the
  7. concentrationconcentrated crude mixture with 2N hydrochloric acid (500 mL)
  8. extractionextract with dichloromethane (3×400 mL)
  9. dry with materialCombine the organic layers, dry over sodium sulfate
  10. filtrationfilter
  11. concentrationconcentrate under reduced pressure
  12. washeluting with 20% ethyl acetate/hexanes
  13. additionCombine fractions containing product
  14. concentrationconcentrate them under reduced pressure