Silver trifluoroacetate

Silver trifluoroacetate Basic information
Product Name:Silver trifluoroacetate
Synonyms:trifluoro-aceticacisilver(1++)salt;SILVER TRIFLUOROACETATE;SILVER(I) TRIFLUOROACETATE;TRIFLUOROACETIC ACID SILVER SALT;SILVER TRIFLUOROACETATE, 99.99+%;Silvertrifluoroacetate,min.98%;Trifluoroacetic acid silver(I) salt;Acetic acid, trifluoro-, silver(1+) salt
CAS:2966-50-9
MF:C2AgF3O2
MW:220.88
EINECS:221-004-0
Product Categories:metal acetate salt;Ag;Organic-metal salt
Mol File:2966-50-9.mol
Silver trifluoroacetate Structure
Silver trifluoroacetate Chemical Properties
Melting point 257-260 °C (dec.) (lit.)
storage temp. Store below +30°C.
form Crystalline Powder
color Light beige to gray
Water Solubility SOLUBLE
Sensitive Hygroscopic
BRN 3634022
CAS DataBase Reference2966-50-9(CAS DataBase Reference)
EPA Substance Registry SystemAcetic acid, trifluoro-, silver(1+) salt (2966-50-9)
Safety Information
Hazard Codes Xi,T,N
Risk Statements 36/38-50-36/37/38
Safety Statements 26-61-36/39
WGK Germany 3
3-8
Hazard Note Toxic/Hygroscopic
TSCA T
HazardClass HYGROSCOPIC, TOXIC
HazardClass 9
HS Code 28432900
MSDS Information
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Silver trifluoroacetate Usage And Synthesis
Chemical Propertieslight beige to grey crystalline powder
UsesSilver Trifluoroacetate functions as a catalyst in the synthesis of cyclobutene-fused azepines/dihydropyridines.
ApplicationSilver trifluoroacetate is the silver salt of trifluoroacetic acid and is used as a Lewis acid catalyst. It is used as an important raw material for the preparation of triethylsilyl trifloroacetate and triphenylmethyl trifluoroacetate. Further, it is used as a catalyst in the preparation of 4-iodoveratrole from veratrole by reacting with iodine.
SynthesisSilver trifluoroacetate is prepared by the reaction of silver oxide and trifluoroacetic acid.
Reaction equation: Ag2O+2CF3COOH→2CF3COOAg+H2O
Reaction: 187g (0.81mol) of silver oxide was weighed and suspended in 200mL of water, and 177g (1.55mol) of trifluoroacetic acid was added. After filtration, the filtrate was evaporated to dryness under reduced pressure. The residue was extracted with ether in a Soxhlet extractor. Alternatively, dissolve the residue in 1.2L of ether and filter through a thin layer of activated carbon. After distilling off the ether, 300g of the product was obtained with a yield of 83%.
Purification MethodsThe extract is filtered and evaporated to dryness, then the powdered residue is completely dried in a vacuum desiccator over silica gel. Its solubility in Et2O is 33.5g in 750mL. It can be recrystallised from *C6H6 (solubility is: 1.9g in 30mL of *C6H6, and 33.5g will dissolve in 750mL of anhydrous Et2O). [Traynham & Dehn J Org Chem 23 1545 1958, Haszeldine J Chem Soc 584 1951.] Store it in the dark. It is also soluble in trifluoroacetic acid (15.2% at 30o), toluene, o-xylene and dioxane [Hara & Cady J Am Chem Soc 76 4285 1954]. [Beilstein 2 IV 461.]
Tosyl azide Silver acetate Sodium anthraquinone-2-sulfonate Ethyl 2-(Chlorosulfonyl)acetate Difluoroacetic acid Ascoric Acid Folic acid Trifluoroacetic acid Glycine SILVER FLUOROACETATE Ethyl trifluoroacetate Sodium trifluoroacetate Silver trifluoroacetate Trifluoroacetic anhydride Mercury Silver phosphoric acid Citric acid

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