Search results
Results from the WOW.Com Content Network
Trifluoroacetic acid in a beaker. TFA is the precursor to many other fluorinated compounds such as trifluoroacetic anhydride, trifluoroperacetic acid, and 2,2,2-trifluoroethanol. [4] It is a reagent used in organic synthesis because of a combination of convenient properties: volatility, solubility in organic solvents, and its strength as an ...
Chemical compatibility is a rough measure of how stable a substance is when mixed with another substance. [1] If two substances can mix together and not undergo a chemical reaction, they are considered compatible. Incompatible chemicals react with each other, and can cause corrosion, mechanical weakening, evolution of gas, fire, or other ...
Triflic acid (CF 3 SO 3 H) and trifluoroacetic acid (CF 3 CO 2 H) are useful throughout organic synthesis. Their strong acidity is attributed to the electronegativity of the trifluoromethyl group that stabilizes the negative charge. The triflate-group (the conjugate base of the triflic acid) is a good leaving group in substitution reactions.
Trifluoroacetic acid is a widely employed acid, used for example in the synthesis of peptides.Its esters are useful in analytical chemistry. Longer-chain perfluoroalkyl carboxylic acids, e.g. with five to nine carbons, are useful fluorosurfactants and emulsifiers used in the production of polytetrafluoroethylene (Teflon) and related fluoropolymers.
Fluoral can be prepared from trifluoroacetic acid with lithium aluminium hydride in diethyl ether: [4] CF 3 COOH + LiAlH 4 → CF 3 CHO + ... or with concentrated sulfuric acid. Cathodic reduction of bromotrifluoromethane in dimethylformamide with aluminium as anode gives high yields of fluoral.
Trifluoroacetic anhydride was originally prepared by the dehydration of trifluoroacetic acid with phosphorus pentoxide. [2] The dehydration might also be carried out with excess α-halogenated acid chlorides. For example, with dichloroacetyl chloride: [3] 2 CF 3 COOH + Cl 2 CHCOCl → (CF 3 CO) 2 O + Cl 2 CHCOOH + HCl
The trifluoromethyl group has a significant electronegativity that is often described as being intermediate between the electronegativities of fluorine and chlorine. [1] For this reason, trifluoromethyl-substituted compounds are often strong acids, such as trifluoromethanesulfonic acid and trifluoroacetic acid.
Copper trifluoroacetate can be obtained by reacting trifluoroacetic acid with copper oxide, copper hydroxide or basic copper carbonate.Acetone can replace the water molecules in copper trifluoroacetate hydrate, and under reduced pressure conditions, the acetone can be removed to obtain anhydrous material.