Sodium chlorodifluoroacetate

Sodium chlorodifluoroacetate

Identifiers
CAS Number	1895-39-2
3D model (JSmol)	Interactive image
ChemSpider	67266
ECHA InfoCard	100.015.988
EC Number	217-586-0
PubChem CID	2734985
UNII	ZAY4J838P2
CompTox Dashboard (EPA)	DTXSID1062049
InChI InChI=1S/C2HClF2O2.Na/c3-2(4,5)1(6)7;/h(H,6,7);/q;+1/p-1 Key: MRTAVLDNYYEJHK-UHFFFAOYSA-M
SMILES C(=O)(C(F)(F)Cl)[O-].[Na+]
Properties
Chemical formula	C2ClF2NaO2
Molar mass	152.46 g·mol−1
Appearance	white solid
Melting point	196–198 °C (385–388 °F; 469–471 K)
Hazards
GHS labelling:[1]
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Sodium chlorodifluoroacetate is the organofluorine compound with the formula CF₂ClCO₂Na.^[2] It is a salt formed by neutralization of chlorodifluoroacetic acid with sodium hydroxide. The compound, a white solid, is of interest as a source of difluorocarbene:

CF₂ClCO₂Na → NaCl + CF₂ + CO₂

This reaction is conducted in a hot solution also containing the substrate. Diglyme is a typical solvent.^[2] The conversion of sodium chlorodifluoroacetate is proposed to start with decarboxylation, which generates the carbanion ClF₂C⁻.

One set of applications is difluorocyclopropanation. Thermal decomposition of sodium chlorodifluoroacetate in the presence of triphenylphosphine and an aldehyde allows for a Wittig-like reactions^[3] In this case, (C₆H₅)₃P=CF₂ is proposed as an intermediate.

References

This page was last edited on 9 May 2024, at 22:21