HRID1270497

反应详情

EQUATION

反应方程式

HRID 1270497 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
55 °C

PROCEDURE

实验过程

A mixture of p-methoxypropiophenone (2.39 g, 14.5 mmol), 90% lead(IV)acetate (6.45 g, 14.5 mmol), triethylorthoformate (15 ml) and 70% perchloric acid (1.2 ml. 29 mmol) was heated to 55° C. for 18 h. The mixture was cooled and the triethylorthoformate removed under reduced pressure. The residue was dissolved in CHCl3 and the remaining precipitate filtered off and discarded. The CHCl3 solution was then washed with water and evaporated to yield the crude ester. This crude ester product was dissolved in a 10% KOH 1:1 water:methanol solution, which was then refluxed for 3 h. After cooling the methanol was evaporated under reduced pressure and the aqueous solution washed with diethylether (3×25 ml). The aqueous solution was acidified with 2N H2SO4, then washed again with diethylether (3×25 ml). The combined fractions from the second ether wash were dried (Na2SO4) and evaporated to give the propionic acid (1.66 g, 63%).

WORKUP

后处理

  1. temperatureThe mixture was cooled
  2. customthe triethylorthoformate removed under reduced pressure
  3. dissolutionThe residue was dissolved in CHCl3
  4. filtrationthe remaining precipitate filtered off
  5. washThe CHCl3 solution was then washed with water
  6. customevaporated
  7. customto yield the crude ester
  8. customwas evaporated under reduced pressure
  9. washthe aqueous solution washed with diethylether (3×25 ml)
  10. washwashed again with diethylether (3×25 ml)
  11. washThe combined fractions from the second ether wash
  12. dry with materialwere dried (Na2SO4)
  13. customevaporated