HRID1806908

反应详情

EQUATION

反应方程式

HRID 1806908 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

Step B To a suspension of CuI (7.61 g, 40 mmol) in anhydrous ethyl ether (20 mL) at 0° C. was added an ethyl ether solution (1.6 M) of MeLi (50 mL, 80 mmol) The reaction mixture was stirred at 0° C. for 10 min. The solvent was evaporated under reduced pressure, then dichloromethane (20 mL) was added under nitrogen at 0° C. The mixture was stirred for 5 min. The solvent was evaporated again. To the residue was added dichlormethane (20 mL), and the temperature of the mixture was lowered to −78° C. To the mixture was added chlorotrimethylsilane (4.3 g, 40 mmol) and a dichloromethane solution (20 mL) of cyclohexylidene-acetic acid methyl ester (3.1 g, 20 mmol). The reaction mixture was allowed to slowly warmed to 0° C. and stirred for 1 h. Aqueous saturated NH4Cl solution was added to quench the reaction. The mixture was extracted with ethyl ether twice. The organic layers were combined, dried over MgSO4, concentrated. The residue was purified by chromatography (EtOAc:hexanes=1:5) to give (1-methyl-cyclohexyl)-acetic acid methyl ester as a colorless oil (3.3 g, 97%).

WORKUP

后处理

  1. customThe solvent was evaporated under reduced pressure
  2. additiondichloromethane (20 mL) was added under nitrogen at 0° C
  3. stirringThe mixture was stirred for 5 min
  4. customThe solvent was evaporated again
  5. additionTo the residue was added dichlormethane (20 mL)
  6. customwas lowered to −78° C
  7. temperatureto slowly warmed to 0° C.
  8. stirringstirred for 1 h
  9. customto quench
  10. customthe reaction
  11. extractionThe mixture was extracted with ethyl ether twice
  12. dry with materialdried over MgSO4
  13. concentrationconcentrated
  14. customThe residue was purified by chromatography (EtOAc:hexanes=1:5)