Summary
Sodium trifluoroacetate is a chemical compound with a formula of CF3CO2Na. It is the sodium salt of trifluoroacetic acid. It is used as a source of trifluoromethylations.[1]
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| Names | |
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| IUPAC name
Sodium trifluoroacetate
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| Other names
Sodium perfluoroacetate
Sodium 2,2,2-trifluoroacetate | |
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3D model (JSmol)
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| ECHA InfoCard | 100.018.982 |
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C2F3NaO2 | |
| Molar mass | 136.005 g·mol−1 |
| Appearance | White crystalline powder |
| Density | 1.49 g mL−1 |
| Melting point | 207 °C (405 °F; 480 K) |
| Boiling point | Decomposes |
| 625 g/L | |
| Solubility | soluble in alcohol, acetonitrile, dimethylformamide and most of polar organic solvents |
| Acidity (pKa) | 0.23 (conjugate acid) |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards
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Toxic, Irritant, Harmful to environment |
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| Danger | |
| H300, H315, H319, H335, H410 | |
| P261, P264, P270, P271, P273, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P391, P403+P233, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | Non-flammable |
| Non-flammable | |
| Related compounds | |
Other anions
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Sodium trichloroacetate |
Other cations
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Lithium trifluoroacetate Potassium trifluoroacetate |
Related compounds
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Sodium formate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Basicity edit
With a pKa of 0.23 for trifluoroacetic acid, the trifluoroacetate ion is an extremely weak base compared to acetic acid, which has a pKa of 4.76. This is due to the electron-withdrawing effect of the three fluorine atoms adjacent the carboxylate group. Strong acids such as hydrochloric acid or sulfuric acid can protonate the trifluoroacetate ion to trifluoroacetic acid:
In general, trifluoroacetate reacts in equilibrium with hydronium cations to form trifluoroacetic acid:
The general reaction with hydronium is in equilibrium due to the similarity in pKa between trifluoroacetic acid and the hydronium ion.
Preparation edit
One convenient method is by dissolving an equivalent amount of sodium carbonate in 50% aqueous solution of trifluoroacetic acid. The solution is filtered and evaporated by vacuum evaporation (with special care to avoid decomposition of the salt by overheating). The solid obtained is dried under vacuum at 100 °C.[2]
Uses edit
Sodium trifluoroacetate is a useful reagent for trifluoromethylation.
The trifluoromethylation process with sodium trifluoroacetate.
See also edit
References edit
- ^ Chang, Ying; Cai, Chun (June 2005). "Trifluoromethylation of carbonyl compounds with sodium trifluoroacetate". Journal of Fluorine Chemistry. 126 (6): 937–940. doi:10.1016/j.jfluchem.2005.04.012.
- ^ Prakash, G. K. Surya; Mathew, Thomas (2010), "Sodium Trifluoroacetate", Encyclopedia of Reagents for Organic Synthesis, doi:10.1002/047084289x.rn01136, ISBN 9780470842898