Trifluoromethane, 46

The silver fluorocomplexes, ie, silver hexafluoroantimonate [26042-64-8], AgSbF silver hexafluorophosphate [26042-63-7], AgPF silver tetrafluoroborate [14104-20-2], AgBF and other salts such as silver trifluoromethane sulfonate [2923-28-6], CF SO Ag, and silver trifluoroacetate [2966-50-9], CF COOAg, play an important role in the synthesis of organic compounds and have gained potential industrial importance. 

Ca.ta.lysis by Protons. The discovery of hydrogen peroxide hydroxylation of phenol in the presence of strong acids such as perchloric, trifluoromethane-sulfonic, or sulfuric acids allows suppression of all previous drawbacks of the process (18,19). This mode of hydroxylation gives high yields (85% based on H2O2 at phenol conversion of 5—6%). It can be mn without solvents and does not generate resorcinol. Its main advantage rehes on... 

Pharmaceuticals and Agrochemicals. Thioglycohc acid and its esters are useful as a raw material to obtain biologically active molecules. In cephalosporine syntheses, (4-pyridyl)thioacetic acid [10351 -19-8] (65) and trifluoromethane (ethyl) thioglycolate [75-92-9] (66) are used as intermediates. Methyl-3-ainino-2-thiophene carboxylate can be used as intermediate for herbicidal sulfonylureas (67) and various thiophenic stmctures (68). 

Trimethylsilyl trifluoromethane (trifluoromethyl trimethylsilane) [81290-20-2] M 142.2, b 54-55°, 55-55.5°, d 0.962, n 1.332. Purified by distilling from trap to trap in a vacuum of 20mm using a bath at 45° and Dry ice-Me2CO bath for the trap. The liquid in the trap is then washed with ice cold H2O (3x), the top layer is collected, dried (Na2S04), the liquid was decanted and fractionated through a helices packed column at atmospheric pressure. H, C, F, and Si NMR can be used for assessing the purity of fractions. [Tetrahedron Lett 25 2195 1984 J Org Chem 56 984 1991.]... 

Tricliloro-l, 2,2-trifluoroethane, 132 Tricresyl phosphates, 132 Tricyclohexyltin hydroxide, 132 Triethyl aluminum, 132 Triethylamine, 132 Triethyl phosphite, 132 Trifluorobromomethane, 132 Trifluoroethane, 132 Trifluoromethane, 132 Trifluralin, 132 Triisobutyl aluminum, 133 Trikem SA, 146... 

In contrast to phosphorus esters, sulfur esters are usually cleaved at the carbon-oxygen bond with carbon-fluorine bond formation Cleavage of esteri nf methanesulfonic acid, p-toluenesidfonic acid, and especially trifluoromethane-sulfonic acid (tnflic acid) by fluoride ion is the most widely used method for the conversion of hydroxy compounds to fluoro derivatives Potassium fluoride, triethylamine trihydrofluoride, and tetrabutylammonium fluoride are common sources of the fluoride ion For the cleavage of a variety of alkyl mesylates and tosylates with potassium fluoride, polyethylene glycol 400 is a solvent of choice, the yields are limited by solvolysis of the leaving group by the solvent, but this phenomenon is controlled by bulky substituents, either in the sulfonic acid part or in the alcohol part of the ester [42] (equation 29)... 

An example of cleavage ol the sulfur-oxygen bond in trifluoromethane-sulfonic ester has been reported Tnfluororaethyl triflate reacts with neutral or anionic nucleophiles with elimination of carbonyl difluoride and formation of trifluoromethanesulfonyl fluoride [57] (equation 32) The mechanism of this reaction involves elimination of fluoride ion, which is a chain carrier in the substitution of fluorine for the trifluoromethoxy group... 

Thermal cleavage of boron tris(trifluoromethane)sulfonate and boron tris(pen-tafluoroethane)sulfonate was studied. Careful identificadon of the products has led to the proposal of a mechanism and an account for this process [121] (equation 93). 

The unique combination of properties associated with certain fluonnated methanes and ethanes has led to their widespread use in fire suppression systems The three halogenated fire suppression agents in general use today are bromo-trifluoromethane (CF Br, Halon 1301), bromochlorodifluoromethane (CF2BtCl, Halon 1211) and, in small volumes, primarily in the republics of the former Soviet Union and Eastern European nations, 1,2-dibromotetrafluoroethane (BrCF2Cp2Br, Halon 2402)... 

Fluorine cannot be used, although trifluoroketones can be cleaved into carboxylate and trifluoromethane. The haloform reaction can be conducted under mild conditions—at temperatures ranging from 0-10 °C—in good yields even a sensitive starting material like methylvinylketone can be converted into acrylic acid in good yield. 

The choice of the anion ultimately intended to be an element of the ionic liquid is of particular importance. Perhaps more than any other single factor, it appears that the anion of the ionic liquid exercises a significant degree of control over the molecular solvents (water, ether, etc.) with which the IL will form two-phase systems. Nitrate salts, for example, are typically water-miscible while those of hexaflu-orophosphate are not those of tetrafluoroborate may or may not be, depending on the nature of the cation. Certain anions such as hexafluorophosphate are subject to hydrolysis at higher temperatures, while those such as bis(trifluoromethane)sulfonamide are not, but are extremely expensive. Additionally, the cation of the salt used to perform any anion metathesis is important. While salts of potassium, sodium, and silver are routinely used for this purpose, the use of ammonium salts in acetone is frequently the most convenient and least expensive approach. 

Chlorodifluoro- Pentafluoroethane Azeotropic Mixture Chlorotrifluoro- Trifluoromethane Azeotrope Azeotrope... 

Anions are just as varied as the cations, and more than 250 different ionic liquids with different anion/cation combinations are commercially available. Hexafluorophosphate, tetrafluoroborate, alkyl sulfates, trifluoromethane-sulfonates (Inflates), and halides are some anion possibilities. 

The interfacial properties of gel electrolytes containing ethylene carbonate immobilized in a polyacrylonitrile (PAN) matrix with a lithium (bis)trifluoromethane sulfonimide (LiTFSI) salt have been studied 1139]. SEI stability appeared to be strongly dependent on the LiTFSI concentration. A minimum value of / SE1 of about 1000 Qcm2 was obtained after 200h... 

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