Abstract: Liquid clathrate compositions useful as reusable aluminum catalysts in Friedel-Crafts reactions are described. In one embodiment, the liquid clathrate composition is formed from constituents comprising (i) at least one aluminum trihalide, (ii) at least one salt selected from alkali metal halide, alkaline earth metal halide, alkali metal pseudohalide, quaternary ammonium salt, quaternary phosphonium salt, or ternary sulfonium salt, or a mixture of any two or more of the foregoing, and (iii) at least one aromatic hydrocarbon compound.

Abstract: A mixture formed from one or more alkyl disulfides, benzene, and at least about 1.5 equivalents of Lewis acid catalyst is heated to form alkanethiobenzene. Reaction in a mixture formed from excess benzene, dimethyldisulfide (DMDS) and AlCl.sub.3 in which the mole ratio of AlCl.sub.3 to DMDS was 2:1 was complete in 2 hours and afforded 98% conversion and 93% yield of thioanisole. In contrast, the same reaction when attempted using a 1:1 mole ratio of AlCl.sub.3 to DMDS after 6 hours achieved only 66% conversion and a thioanisole yield of only 35%. So far as is known, this is the first example of a highly efficient electrophilic aromatic substitution of the inactivated benzene ring by an alkanethio group.

Abstract: Described are novel processes which employ reusable aluminum catalysts in Friedel-Crafts reactions.

Abstract: Improved process for separating ethylsilane from silane by selective adsorption onto an effectively treated carbon bed and method of treatment of such carbon bed to enhance the selective adsorption of ethylsilane.

Abstract: Non-solvated hydridomagnesium chloride is prepared in high yield under moderate conditions by reacting magnesium hydride and magnesium chloride in a hydrocarbon solvent and in the presence of a trialkylaluminum catalyst.

Abstract: Improved molecular sieves and processes for treatment of molecular sieves which permit use for separation of ethylene and silane without attending formation of ethylsilane. Such treatment includes treatment of sieves with silane at an effective temperature, pressure and time.

Abstract: A process for preparing a silane mixture of the formulaSi R.sub.n X.sub.4-nwhere R is C.sub.1 to C.sub.12 linear or branched alkyl, phenyl or phenyl substituted with one or more C.sub.1 to C.sub.6 linear or branched alkyl; X is chloro, bromo or iodo; and n is an integer from 1 to 4; comprising reacting silicon tetrafluoride with metallic aluminum and RX, where R and X are as previously described, at a temperature of about 150.degree. C. to about 400.degree. C.

Abstract: A process for preparing a silane mixture of the formulaSiR.sub.n X.sub.4-nwhere R is C.sub.1 to C.sub.12 linear or branched alkyl, phenyl or phenyl substituted with one or more C.sub.1 to C.sub.6 linear or branched alkyl; X is chloro, bromo or iodo; and n is an integer from 1 to 4; comprising reacting silicon tetrafluoride with (R).sub.3 Al.sub.2 X.sub.3, where R and X are as previously described, at a temperature of about 325.degree. C. to about 360.degree. C.

Abstract: Tertiary amine alanes are produced by reacting sodium aluminum hydride and magnesium dichloride. A tertiary amine is admixed to extract the tertiary amine alane. Stoichiometric ratios of sodium aluminum hydride to magnesium dichloride can be varied to effect the magnesium compound by-product produced.

Abstract: A process for selective reduction is provided wherein an organic compound containing a reducible group such as acid, acid chloride, ester, aldehyde, ketone, epoxide, amide, oxime, imine, nitrile, or the like, is reacted with a tertiary amine alane such that an alcohol or an amine is produced, substantially without reduction of another group in the molecule such as a halogen-containing functionality, nitro group, or double bond.

Abstract: Improved processes for the production of silane. Hydridomagnesium chloride and trichlorosilane are reacted in an ether solvent to co-produce silane and magnesium chloride. Recycle schemes are presented for the recovery of magnesium values.

Abstract: Lithium aluminum hydride reacts with a tertiary amine to produce an amine alane and Li.sub.3 AlH.sub.6. Lithium values are recycled by reacting Li.sub.3 AlH.sub.6 with aluminum and hydrogen to produce LiAlH.sub.4. Since no metal halide by-product is produced in the first step, it has an advantage over other routes. The amine alane can react with SiF.sub.4 to produce silane and AlF.sub.3.