HRID863154

反应详情

EQUATION

反应方程式

HRID 863154 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
65 °C

PROCEDURE

实验过程

Allyl (1S,2R,3S)-3-(4-methoxy-2-methoxymethoxyphenyl)-1-(3,4-methylenedioxyphenyl)-5-(prop-1-yloxy)indane-2-carboxylate (1.7 g, 3.11 mmol) was dissolved in allyl alcohol (20 ml) and then 15 drops of conc. HCl was added. The resulting solution was stirred at 65° C. for 2 h. After removing the solvent the residue was partitioned between water and ethyl acetate. The organic layers were washed with water, 5% aqueous NaHCO3 and brine; then dried (MgSO4 anhyd.), filtered and evaporated to give an oil. The product was purified by column chromatography to provide the title compound as a pale yellow oil (1.26 g, 81%).

WORKUP

后处理

  1. customAfter removing the solvent the residue
  2. customwas partitioned between water and ethyl acetate
  3. washThe organic layers were washed with water, 5% aqueous NaHCO3 and brine
  4. dry with materialthen dried (MgSO4 anhyd.)
  5. filtrationfiltered
  6. customevaporated
  7. customto give an oil
  8. customThe product was purified by column chromatography