HRID225405
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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 2-benzoyloxy-1,1,3,3,3-pentafluoro-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
- customsynthesized in Synthesis Example 9
- customThe organic layer was separated
- washwashed with 50 g of water three times
- concentrationThe organic layer was concentrated
- addition25 g of diethyl ether was added to the residue for crystallization
- filtrationThe crystals were filtered
- customdried
- customobtaining the target compound