HRID987235

反应详情

EQUATION

反应方程式

HRID 987235 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Tetramethylguanidine (6.5 g; 56.6 mmole) was slowly added to a solution of 3-benzyloxybenzaldehyde (11.7 g; 55 mmole) and (1,2-diethoxy-2-oxoethyl)(triphenyl) phosphonium chloride (20.1 g; 46.8 mmole) in dichloromethane (200 ml) at 0° C. After stirring at room temperature overnight the solvent was evaporated in vacuo. Diethyl ether was added and insoluble material was filtered off. The filtrate was washed with sodium bicarbonate solution, dried (magnesium sulfate), filtered and the solvent was evaporated in vacuo. The residue was purified by chromatography on silica gel using tetrahydrofuran (0.5%) in dichloromethane as eluant. The remaining aldehyde was removed by stirring with sodium bisulfite in water and diethyl ether for 2 days. The phases were separated and the organic phase was evaporated in vacuo to give 10.5 g (yield 69%) of 3-(3-benzyloxyphenyl)-2-ethoxyacrylic acid ethyl ester.

WORKUP

后处理

  1. customwas evaporated in vacuo
  2. additionDiethyl ether was added
  3. filtrationinsoluble material was filtered off
  4. washThe filtrate was washed with sodium bicarbonate solution
  5. dry with materialdried (magnesium sulfate)
  6. filtrationfiltered
  7. customthe solvent was evaporated in vacuo
  8. customThe residue was purified by chromatography on silica gel
  9. customThe remaining aldehyde was removed
  10. stirringby stirring with sodium bisulfite in water and diethyl ether for 2 days
  11. customThe phases were separated
  12. customthe organic phase was evaporated in vacuo