Silanes reaction with metal halides

Perfluoroalkylcopper reagents are the most studied perfluoroalkyl organometallic reagents due to their unique combination of thermal stability and chemical reactivity. They are readily prepared by copper metal insertion reactions with perfluoroalkyl halides in a coordinating solvent (e.g., formation of decarboxylation reactions of perfluoroalkanoic acid salts and copper(I) halide (e.g., formation of 2 ), or metathesis reactions (e.g., formation of 4 via 3 ). (Trifluoro-methyl)copper (4) has also been recently accessed by decomposition of methyl 2,2-difluoro-2-(fluorosulfonyl)acetate (5) or methyl perfluoro [2-(fluorosulfonyl)ethoxy]acetate (6) in the presence of copper(I) iodide and by reaction of trimethyl(trifluoromethyl)silane (7) with fluoride and copper(I) iodide. ... 

Silica is reduced to silicon at 1300—1400°C by hydrogen, carbon, and a variety of metallic elements. Gaseous silicon monoxide is also formed. At pressures of >40 MPa (400 atm), in the presence of aluminum and aluminum halides, silica can be converted to silane in high yields by reaction with hydrogen (15). Silicon itself is not hydrogenated under these conditions. The formation of silicon by reduction of silica with carbon is important in the technical preparation of the element and its alloys and in the preparation of silicon carbide in the electric furnace. Reduction with lithium and sodium occurs at 200—250°C, with the formation of metal oxide and silicate. At 800—900°C, silica is reduced by calcium, magnesium, and aluminum. Other metals reported to reduce silica to the element include manganese, iron, niobium, uranium, lanthanum, cerium, and neodymium (16). 

This is a reaction that seems veiy attractive for synthesis but, in the absence of a transition met catalyst, the yields are very low. We showed in the last chapter how vinyl silanes can be made wit control over stereochemistry and converted into lithium derivatives with retention. Neither of thes vinyl metals couple with vinyl halides alone. But in the presence of a transition metal—Cu (I) for I and Pd(0) for Sn—coupling occurs stereo specifically and in good yield. 

The intermediate metal hydride has been isolated on occasion for Co and Mn , and Eq. (b) has actually been used to prepare silicon-metal bonds (see 5.2.3.2.2.). Inspection of Table 1 reveals the ease of reaction of Co2(CO)g compared with the other carbonyls. Normally this reaction is performed simply by condensing volatile silane onto the carbonyl in the absence of solvent and then allowing rapid reaction in the liquid phase at room temperature, but for the remaining carbonyls it is necessary to use elevated temperatures and sealed, evacuated tubes. The products are volatile and readily purified by vacuum fractionation or sublimation, but are often oxygen and moisture sensitive. The route is most efficient for RjSi derivatives of Co, Mn and Re, which are not generally obtainable by the reactions of silicon halides with metal carbonyl anions (see S.8.3.3.I.). In this way lCo(SiR,)(CO -] = Et, Phj, Clj -, (OEt)j, F/, ... 

The most useful of all allyl anion equivalents are the allyl silanes.20 This is because it is easy to make them regioselectively, because they do not undergo allylic rearrangement (silicon does not do a [1,3] shift) and because their reactions with electrophiles are very well controlled addition always occurring at the opposite end to the silicon atom. Symmetrical allyl silanes can be made from allyl-lithiums or Grignards by displacement of chloride from silicon. A useful variant is to mix the halide with a metal, e.g. sodium, and Me3SiCl in the same reaction, rather after the style of the silicon acyloin reaction,21 as in the synthesis of the acetal 80. 

Cross-coupling Reactions. Trimethylsilylmethylmagnesium chloride reacts with organic halides (or pseudohalides), especially aryl and alkenyl halides, in the presence of transition metal catalysts. The reactions directly provide allylic or benzylic trimethyl-silanes of significant synthetic use. 

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