تفاعل #2186216
ord-4f580f2eefde42d5824fdb0dd052f5ab
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىsynthesized in Synthesis Example 10
- 2أخرىto quench
- 3أخرىthe reaction
- 4workup.DISTILLATIONThe methanol was distilled off in vacuum
- 5workup.ADDITIONafter which 270 g of dichloromethane was added to the residue
- 6غسيلThe organic layer was washed with 40 g of water three times
- 7تركيزThe organic layer was concentrated
- 8workup.ADDITION60 g of diethyl ether was added to the
- 9تركيزconcentrate for crystallization
- 10ترشيحThe crystals were filtered
- 11أخرىdried
- 12أخرىobtaining the target compound
الإجراء التجريبي
In 72 g of methanol was dissolved 34.4 g of triphenylsulfonium 2-benzoyloxy-1,1,3,3,3-pentafluoropropane-1-sulfonate synthesized in Synthesis Example 10. While the solution was stirred under ice cooling, 54.0 g of 5% sodium hydroxide solution was added dropwise at a temperature below 10° C. It was allowed to mature at the temperature for 4 hours. At a temperature below 10° C., 6.8 g of 12N hydrochloric acid was added to quench the reaction. The methanol was distilled off in vacuum, after which 270 g of dichloromethane was added to the residue. The organic layer was washed with 40 g of water three times. The organic layer was concentrated, and 60 g of diethyl ether was added to the concentrate for crystallization. The crystals were filtered and dried, obtaining the target compound. White crystals, 24.3 g (yield 85%).