HRID14495

反应详情

EQUATION

反应方程式

HRID 14495 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 2-(4-chlorophenyl)-1-(2,4-dihydroxyphenyl)-ethanone (100 g, 0.382 mol), iso-butyric acid anhydride (380 ml, 2.29 mol) and dry pyridine (380 ml, 4.69 mol) is stirred at 140° C. for 12 h and then allowed to cool to room temperature. The volatile components are removed in vacuo, and the resulting dark brown oil is dried under high vacuum to give crude isobutyric acid 3-(4-chlorophenyl)-2-isopropyl-4-oxo-4H-chromen-7-yl ester. To a mixture of this crude ester and methanol (400 ml) is added aqueous KOH (250 ml, 5 M) [CAUTION: EXOTHERM]. The dark solution is stirred for 1.5 h, and the methanol is then evaporated in vacuo. The resulting solution is acidified with 2 M HCl to pH 3 to give a brown precipitate, which is removed by filtration. The brown solid is washed with water (3×) and isopropyl ether and then air-dried. The remaining aqueous solution is extracted with ethyl acetate (4×), and the combined organic phases are washed with water (3×), dried (Na2SO4) and evaporated to give a red oil, which solidifies to give a brown solid. The brown solid is washed with isopropyl ether and air-dried. The combined aqueous phases are extracted again (ethyl acetate) to provide a third crop of product.

WORKUP

后处理

  1. customthe methanol is then evaporated in vacuo
  2. customto give a brown precipitate, which
  3. customis removed by filtration
  4. washThe brown solid is washed with water (3×) and isopropyl ether
  5. customair-dried
  6. extractionThe remaining aqueous solution is extracted with ethyl acetate (4×)
  7. washthe combined organic phases are washed with water (3×)
  8. dry with materialdried (Na2SO4)
  9. customevaporated
  10. customto give a red oil, which
  11. customto give a brown solid
  12. washThe brown solid is washed with isopropyl ether
  13. customair-dried
  14. extractionThe combined aqueous phases are extracted again (ethyl acetate)
  15. customto provide a third crop of product