From halo sulfones

Strongest evidence for a rapid equilibration of the a-halo sulfone with its a- and a -anions comes from reactions performed in D2O. If such reactions are interrupted before they are complete, the recovered a-halo sulfones are almost fully deuterated at both the a- and a -positions. Furthermore, the alkene products are also essentially fully deuterated, this time at the vinylic positions. When allowed to run to completion, this forms the basis of a very useful preparative method for deuterium-labeled alkenes (Scheme 8 and equation 24). Not only is a high percentage incorporation possible, but the source of deuterium is very cheap. 

The 2-oxyallyl cation has found a number of applications in organic synthesis. These species can be produced from a,a -dibromoketones, from a-halo-trialkylsilyl enol ethers or from allyl sulfones and a Lewis acid. For example, the 2-oxyallyl cation 192 can be prepared from the dibromide 191 and its cycloaddition with furan gave the adduct 193, used in a synthesis of nonactic acid (3.127). These reactions may take a concerted or a stepwise course, depending on the nature of the diene and the allyl cation and the reaction conditions. 

Similarly, 5-thiazole alkanoic acids and their salts are obtained from thioamides and /3-halo -y-keto acids (695). Thus thioarylamides condensed with 3-aroyl-3-bromopropionic acid (88) in isopropanolic solution in the presence of Na COs give first 4-hydroxy-2-aryl-A-2-thiazoline-5-acetic acid intermediates (89), which were dehydrated in toluene with catalytic amounts of p-toluene sulfonic acid to 2,4-diaryl-5-thiazole acetic acid (90) (Scheme 39) (657), with R = H or Me Ar = Ph, o-, m- or p-tolyl, o-, m-, or P-CIC6H4, 0-, m-, or p-MeOC(iH4, P-CF3C6H4, a-thienyl, a-naphthyl (657). 

Trialkylboranes react rapidly and in high yields with a-halo ketones,a-halo esters, a-halo nitriles, and a-halo sulfonyl derivatives (sulfones, sulfonic esters, sulfonamides) in the presence of a base to give, respectively, alkylated ketones, esters, nitriles, and sulfonyl derivatives. Potassium tert-butoxide is often a suitable base, but potassium 2,6-di-tert-butylphenoxide at 0°C in THF gives better results in most cases, possibly because the large bulk of the two tert-buXy groups prevents the base from coordinating with the R3B. The trialkylboranes are prepared by treatment of 3 mol of an alkene with 1 mol of BH3 (15-16). With appropriate boranes, the R group transferred to a-halo ketones, nitriles, and esters can be vinylic, or (for a-halo ketones and esters) aryl. " °... 

Formation of Alkyl Halides from Esters of Sulfuric and Sulfonic Acids Halo-de-suffonyloxy-substitution, etc. 

It is not possible to dissolve the asphaltenes in water by treatment of the halo derivatives with aqueous sodium hydroxide or with aqueous sodium sulfite (II). The hydrolyzed products remained insoluble even in a strongly alkaline solution. The decreased (H + Cl)/C ratios and the increased O/C ratios of the products relative to those of the parent halo-asphaltenes indicate that partial reaction occurs. The infrared spectra of the products showed a broad band centered at 3450 cm 1, a region assigned to the presence of hydroxyl groups in the products, but it was not possible to establish conclusively the presence of sulfonic acid group(s) in the product from the sodium sulfite reaction by assignment of infrared absorption bands to this particular group. 

The replacement of halogen by alkyl or aryl groups is included in this section. For the conversion of RX RH (X = halo) see Section 160 (Hydrides from Halides and Sulfonates). 

Commercial lecithin is produced by water degumming (precipitation from oil with ion-exchange treated water), separation by stacked disk centrifuge, and vacuum drying to less than 1 percent moisture content. Crude lecithins contain 70-72 percent acetone insolubles (AI) and are standardized to 62-64 percent and an acid value of 30 by addition of oil and fatty acids before sale. Crude lecithins may be treated with acetone to obtain free-flowing powders with 95-98 percent AI. Lecithin can be additionally purified, bleached, fractionated, hydrogenated, hydrox-ylated, acetylated, sulfonated, and halo-genated.104 One domestic company makes 13 kinds of lecithin for food uses alone. 

Salts of sulfinic acids ace converted to sulfones by the action of pri-lary/ secondary, and benzyl halides, alkyl sulfates, and aryl halides in which the halogen atoms are activated by nitro groups in the ortbo or para positions. The reaction fails with t-amyl halide. The yields vary widely, depending upon the nature of the reactants. From salts of benzenesulfinic acid and simple alkylating agents, sulfones are produced in 50-90% yields. Satisfactory results have been obtained when the aryl sulfinic acid contains nitro, cyano, and acetamido groups. Keto sulfones are made in 48-62% yields by alkylation with a-halo ketones. ... 

In the same way as enantiomerically pure a-halo ketones, a-halo esters have been prepared in high diastereomeric excesses by asymmetric halogenation of silyl ketene acetals generated from chiral esters So, a successfull procedure was first introduced in 1985, by W. Oppolzer (refs. 8,9), using derivatives of camphor-10-sulfonic acid as chiral auxiliaries (Fig. 4). 

The best preparative method for mercaptopyrimidines varies from position to position from thioureas and their equivalents. Thiones in any of the electrophilic positions are prepared by thiolysis of halo-pyrimidines, or commonly by thiation of pyrimidinones using phosphorus pentasulfide or, more recently, the superior Lawesson reagent 2,4-bis-/ -methoxyphenyl-l,3,2,4-dithiadiphosphetane 2,4-disulfide. Thiolysis in the 5-position requires a metal sulfide and a 5-bromide under vigorous conditions. Alternatively, pyrimidines substituted with strongly electron-donating substituents may be sulfonated, for example, by chlorosulfonic acid, in the 5-position with subsequent reduction to thiol. 

Alcohols with a nucleofuge leaving group in the r-position can be cyclized to give oxetanes. Thus the cyclodehydrohalogenation of halo alcohols occurs in an analogous way to the oxirane synthesis from y -halogenated alcohols (see p 20). Oxetanes can be prepared from 1,3-diols via monoarene sulfonates ... 

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