Identification | More | [Name]
Silver trifluoroacetate | [CAS]
2966-50-9 | [Synonyms]
SILVER(I) TRIFLUOROACETATE SILVER TRIFLUOROACETATE TRIFLUOROACETIC ACID SILVER SALT trifluoro-aceticacisilver(1++)salt Trifluoroacetic acid silver(I) salt SILVER TRIFLUOROACETATE, 99.99+% Silvertrifluoroacetate,min.98% Acetic acid, trifluoro-, silver(1+) salt Silver trifluoroacetate 98% Silvertrifluoroacetate98% Silver 2,2,2-trifluoroacetate Silver trifluoroacetate, min. 98% Trifluoroacetoxysilver(I) | [EINECS(EC#)]
221-004-0 | [Molecular Formula]
C2AgF3O2 | [MDL Number]
MFCD00013199 | [Molecular Weight]
220.88 | [MOL File]
2966-50-9.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xi,T,N | [Risk Statements ]
R36/38:Irritating to eyes and skin . R50:Very Toxic to aquatic organisms. R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S61:Avoid release to the environment. Refer to special instructions safety data sheet . S36/39:Wear suitable protective clothing and eye/face protection . | [WGK Germany ]
3
| [F ]
3-8 | [Hazard Note ]
Toxic/Hygroscopic | [TSCA ]
T | [HazardClass ]
9 | [HazardClass ]
HYGROSCOPIC, TOXIC | [HS Code ]
28432900 |
Hazard Information | Back Directory | [Chemical Properties]
light beige to grey crystalline powder | [Uses]
Silver Trifluoroacetate functions as a catalyst in the synthesis of cyclobutene-fused azepines/dihydropyridines. | [Application]
Silver 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. | [Synthesis]
Silver 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 Methods]
The 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.] |
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