Sodium trifluoromethanesulfinate
Appearance
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Names | |
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Preferred IUPAC name
Sodium trifluoromethanesulfinate | |
Identifiers | |
3D model (
JSmol ) |
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ChemSpider | |
ECHA InfoCard
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100.203.570 |
PubChem CID
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CompTox Dashboard (EPA)
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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).
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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
- Simon Hadlington (2011-08-15). "Trifluoromethylation made easy". RSC Chemistry World.