HRID23656

反应详情

EQUATION

反应方程式

HRID 23656 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

5

PROCEDURE

实验过程

To a stirred solution of 1.32 g of 3-[2-(2-methoxyethoxy)ethoxy]benzaldehyde and 15 mg of tetra-n-butylammonium bromide in 15 ml of CH2Cl2 is added a solution of 2.4 g of trimethylsulfonium methylsulfate in 4 ml of water, followed by 10 ml of 50% NaOH. The mixture is stirred and refluxed for 4 h, then cooled, diluted with ether and brine, and filtered. The organic phase is washed with brine, dried (MgSO4), and concentrated under reduced pressure to provide 1.78 g of the title compound as a pale yellow oil.

WORKUP

后处理

  1. temperaturerefluxed for 4 h
  2. temperaturecooled
  3. filtrationfiltered
  4. washThe organic phase is washed with brine
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated under reduced pressure