تفاعل #1727273

ord-ebf383a0bc364506887e5d68a3af94c0

معادلة التفاعل

CCCCC(=O)OCC(F)(F)S(=O)(=O)[O-].[Na+]
sodium 1,1-difluoro-2-(valeryloxy)ethanesulfonate
[Cl-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium chloride
[Cl-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium chloride
CCCCC(=O)OCC(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
triphenylsulfonium 1,1-difluoro-2-(valeryloxy)ethanesulfonate

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصThen, extraction
  2. 2
    workup.ADDITIONby adding 30 mL of chloroform
  3. 3
    غسيلThe obtained organic layer was rinsed two times with water
  4. 4
    workup.DISTILLATIONby distilling a solvent off,

الإجراء التجريبي

A 100 mL reactor was charged with 3.0 g (26% purity, 2.9 millimoles) of sodium 1,1-difluoro-2-(valeryloxy)ethanesulfonate obtained in Example 5-3 and 30 g of water, followed by adding dropwise an aqueous solution of triphenylsulfonium chloride [17.8 g (5.2 millimoles/1.8 equivalents) of triphenylsulfonium chloride and 16.2 g of water] at room temperature, followed by stirring at room temperature for 1.5 hours. Then, extraction was conducted by adding 30 mL of chloroform. The obtained organic layer was rinsed two times with water, followed by distilling a solvent off, thereby obtaining 0.96 g of the target triphenylsulfonium 1,1-difluoro-2-(valeryloxy)ethanesulfonate.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08110711B2uspto-grants-2012_02