HRID1788346

反应详情

EQUATION

反应方程式

HRID 1788346 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To 50 g of dichloromethane were added an amount (corresponding to 0.011 mole) of the triphenylsulfonium chloride aqueous solution of Synthesis Example 1 and 3.6 g (0.01 mole) of sodium 1,1,3,3,3-pentafluoro-2-benzoyloxy-propane-1-sulfonate synthesized in Synthesis Example 9, followed by stirring. The organic layer was separated and washed with 50 g of water three times. The organic layer was concentrated and 25 g of diethyl ether was added to the residue for crystallization. The crystals were filtered and dried, obtaining the target compound. White crystals, 4.5 g (yield 75%).

WORKUP

后处理

  1. customsynthesized in Synthesis Example 9
  2. customThe organic layer was separated
  3. washwashed with 50 g of water three times
  4. concentrationThe organic layer was concentrated
  5. addition25 g of diethyl ether was added to the residue for crystallization
  6. filtrationThe crystals were filtered
  7. customdried
  8. customobtaining the target compound