Sulfones applications

Amoco developed polybutene olefin sulfonate for EOR (174). Exxon utilized a synthetic alcohol alkoxysulfate surfactant in a 104,000 ppm high brine Loudon, Illinois micellar polymer small field pilot test which was technically quite successful (175). This surfactant was selected because oil reservoirs have brine salinities varying from 0 to 200,000 ppm at temperatures between 10 and 100°C. Petroleum sulfonate applicability is limited to about 70,000 ppm salinity reservoirs, even with the use of more soluble cosurfactants, unless an effective low salinity preflush is feasible. 

Results from electroless copper, tin-lead (solder) fluoborlc and tin-lead (solder) sulfonic applications will be discussed as they bscome available from installations planned for June and July, 1989. 

M.J. Bowden and L.F. Thompson, Electron irradiation of poly(olefin sulfones) Application to electron beam resists, J. Appl. Polym. Sci. 17, 3211 (1973). 

Bowden and L.F. Thompson, Electron irradiation of poly(olefin sulfones) Application to electron beam resists, J. Electrochem. Soc. 120, 1722 (1973) Poly(Styrene sulfone) A sensitive ion millahle positive electron beam resist, J. Electrochem Soc. 121, 1620 (1974) D.R. McKean, U.P. Schaedeli, and S.A. MacDonald, Acid photogeneration from sulfonium salts in solid polymer matrices, J. Polym. Set Polym. Chem. Ed. 27, 3927 (1989) D.R. McKean, U.P. Schaedeli, P.H. Kasai, and S.A. MacDonald, The effect of polymer structure on the efficiency of acid generation from triarylsulfonium salts, J. Polym. Sci. Polym. Chem. Ed. 29, 309 (1991). 

Fjelde, L, T. Austad, HPLC analysis of salt tolerant mixtures of ethoxylated and non-ethoxy-lated sulfonates applicable in enhanced oil recovery. Colloids Swf. A, 1994,82, 85-90. 

Industrial Applications. Perfluoroacylbenzene sulfonates, used as additives in fire-extinguishing compounds and galvanizing baths have been prepared (88). Perfluoroacylbenzenesulfonate salts prepared by Friedel-Crafts reaction of perfluoroacyl haUdes and benzene, and subsequent sulfonation have been used as surfactants (89). 

Other Applications. Hydroxylamine-O-sulfonic acid [2950-43-8] h.2is many applications in the area of organic synthesis. The use of this material for organic transformations has been thoroughly reviewed (125,126). The preparation of the acid involves the reaction of hydroxjlamine [5470-11-1] with oleum in the presence of ammonium sulfate [7783-20-2] (127). The acid has found appHcation in the preparation of hydra2ines from amines, aUphatic amines from activated methylene compounds, aromatic amines from activated aromatic compounds, amides from esters, and oximes. It is also an important reagent in reductive deamination and specialty nitrile production. 

Methane Sulfonic Acid (MSA), Properties, Reactions and Applications, Technical Bulletin PB-70-1A, Elf Atochem North America, Philadelphia, Pa., 1993. 

The most common leaving groups are sulfonate esters and halides. For the sake of convenience, the discussion of certain dehalogenation reactions is also included in this section even though they may not involve 8 2 type displacement. Benzylic alcohols are also known to be displaced by hydrides or deuterides, but there is no evidence for the application of these reactions to the steroid field. 

Some advantages of this reaction are high yield if the tosylate is in a sterically accessible position excellent isotopic purity of the product (usually higher than-95%) and perhaps most important, access to stereospecifically labeled methylene derivatives. For example, deuteride displacement of 3j -tosylates (183) yields the corresponding Sa-d derivative (185) in 96-98% isotopic purity. Application of this method to the labeled sulfonate (184), obtained. by lithium aluminum deuteride reduction of a 3-ketone precursor (see section HI-A) followed by tosylation, provides an excellent synthesis of 3,3-d2 labeled steroids (186) without isotopic scrambling at the adjacent positions. The only other method which provides products of comparable isotopic purity at this position is the reduction of the tosyl-hydrazone derivative of 3-keto steroids (section IV-B). 

This simplified procedure gives the sulfonic acid in very good yield, however the same procedure is not applicable to the synthesis of triflic acid, which would require the synthesis of trifluoromethyllifhium. This procedure also is not applicable to the preparation of the sulfonic acids requiring the use of perfluoropropyl or isopropyllithium intermediates... 

Trimethylsilyl trifluoromethanesulfonate (trimethylsilyl triflate) is the most synthetically useful representative of the family of trialkylsilyl perfluoroalkane-sulfonates (for a review, see reference 101) This reagent is commercially available or can be prepared easily by the reaction of chlorotrimethylsilane and triflic acid [101] It has wide application in organic synthesis as an excellent silylating reagent... 

The addition of secondary amines to acetylenes is most applicable to the synthesis of conjugated acyclic enamines (50,171,172). Particularly the addition to acetylenic esters and sulfones has been investigated (173-177) and it appears that an initial trans addition is followed by isomerization to more stable products where the amine and functional group are in a trans orientation (178). Enamines have also been obtained by addition of secondary amines to allenes (179). 

Metal halide salts other than sodium iodide have been used sparsely to prepare halodeoxy sugars from sulfonate esters. Lithium chloride (107) and lithium bromide (33) have found limited application. Potassium fluoride (dihydrate) in absolute methanol has been used (51, 52) to introduce fluorine atoms in terminal positions of various D-glucose derivatives. The reaction is conducted in sealed tube systems and requires... 

Polysulfone It is a high performance amorphous plastic that is tough, highly heat resistant, strong and stiff. Products are transparent and slightly clouded amber in color. Material exhibits notch sensitivity and is attacked by ketones, esters, and aromatic hydrocarbons. Other similar types in this group include polyethersulfone, polyphenyl-sulfone, and polyarylsulfone. Use includes medical equipment, solar-heating applications and other performance applications where flame retardance, autoclavability and transparency are needed. 

SS/MA may be structured in different ratios of sulfonated styrene to maleic anhydride. Typically, it is 3 1 (20,000 MW) or 1 1 (15,000 MW). The application rates of all calcium phosphate scale/sludge inhibitors or stabilizers vary, based on the amount of calcium present in the cooling system, with increased calcium hardness leading to higher levels of polymer required. 

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