Sodium trifluoroacetate is a chemical compound with a formula of CF<sub>3</sub>CO<sub>2</sub>Na. It is the sodium salt of trifluoroacetic acid. It is used as a reagent in synthetic organic chemistry.
With a pK<sub>a</sub> of 0.23 for trifluoroacetic acid, the trifluoroacetate ion is an extremely weak base compared to acetic acid, which has a pK<sub>a</sub> 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 pK<sub>a</sub> between trifluoroacetic acid and the hydronium ion.
One convenient method is by dissolving an equivalent amount of sodium carbonate in a 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 100âÂÂðC.
Sodium trifluoroacetate is a useful reagent for trifluoromethylation.