Sodium trifluoromethanesulfinate

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Sodium trifluoromethanesulfinate
Structure of sodium trifluoromethylsulfinate
Names
Preferred IUPAC name
Sodium trifluoromethanesulfinate
Identifiers
3D model (
JSmol
)
ChemSpider
ECHA InfoCard
100.203.570 Edit this at Wikidata
  • InChI=1S/CHF3O2S.Na/c2-1(3,4)7(5)6;/h(H,5,6);/q;+1/p-1
    Key: KAVUKAXLXGRUCD-UHFFFAOYSA-M
  • InChI=1/CHF3O2S.Na/c2-1(3,4)7(5)6;/h(H,5,6);/q;+1/p-1
    Key: KAVUKAXLXGRUCD-REWHXWOFAL
  • [Na+].FC(F)(F)S([O-])=O
Properties
CF3NaO2S
Molar mass 156.05 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Sodium trifluoromethanesulfinate (CF3SO2Na) is the sodium salt of trifluoromethanesulfinic acid. Together with

free radical mechanism.[1]

This reagent is also able to trifluoromethylate electron-deficient aromatic compounds under biphasic conditions.[2] Zinc difluoromethanesulfinate, a related polymeric coordination complex, is able to introduce difluoromethyl groups (CHF2-) onto aromatic compounds under similar biphasic conditions as well.[3]

With the use of DMSO as an oxidant, it provides an environmentally friendly way for the synthesis of β-trifluoromethyl alcohols from alkenes.[4]

References

Further reading