تفاعل #312588

ord-6f7f33b144804d3d98407aa7de735403

معادلة التفاعل

[Na+].[OH-]
sodium hydroxide
O=C(OC(C(F)(F)F)C(F)(F)S(=O)(=O)[O-])c1ccccc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium 2-benzoyloxy-1,1,3,3,3-pentafluoropropane-1-sulfonate
Cl
hydrochloric acid
O=S(=O)([O-])C(F)(F)C(O)C(F)(F)F.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium 2-hydroxy-1,1,3,3,3-pentafluoropropane-1-sulfonate
المردود 85.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىsynthesized in Synthesis Example 10
  2. 2
    أخرىto quench
  3. 3
    أخرىthe reaction
  4. 4
    workup.DISTILLATIONThe methanol was distilled off under vacuum, and 270 g of dichloromethane
  5. 5
    workup.ADDITIONwas added
  6. 6
    غسيلThe organic layer was washed with 40 g of water three times
  7. 7
    تركيزThe organic layer was then concentrated
  8. 8
    workup.ADDITION60 g of diethyl ether was added to the residue for crystallization
  9. 9
    ترشيحThe crystals were filtered
  10. 10
    أخرىdried
  11. 11
    أخرىobtaining 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 stirring under ice cooling, 54.0 g of a 5% sodium hydroxide aqueous solution was added dropwise to the solution at a temperature below 10° C. The reaction solution was aged 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 under vacuum, and 270 g of dichloromethane was added. The organic layer was washed with 40 g of water three times. The organic layer was then concentrated and 60 g of diethyl ether was added to the residue for crystallization. The crystals were filtered and dried, obtaining the target compound. White crystals, 24.3 g (yield 85%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07556909B2uspto-grants-2009_07