Methane, reaction with aluminum

All three hydroxo species [M(OEP)(Me)(OH)] (M = P, As, Sb]) are sufficiently acidic to react with the aluminum porphyrin complex Al(OEP)Me, which is known to eliminate methane on reaction with protic reagents. Three novel binuclear... 

Bromofluoromenthane has been prepared in high yield using a one-step reaction with bromine, hydrogen fluoride and methane in the presence of an aluminum trifluoride fluidized bed or fluorinated aluminum catalysts optionally containing cobalt or nickel between 450 and 500°C.20... 

Most of the investigations into disproportionation reactions have mainly concentrated on chlorofiuoro derivatives of methane and ethane. When trichlorofluoromethane is refluxed with aluminum trichloride or aluminum tribromide, dichlorodifluoromethane and carbon tetrachloride are obtained. Dichlorofluoromethane yields chlorodifiuoromethane and chloroform chlorofiuoro derivatives of ethane and longer chain homologs exhibit a tendency towards isomerization as well as disproportionation, i.e. intramolecular halogen atom exchange. In this case, both types of reaction take place simultaneously. In other words, disproportionation of l,l,2-triehloro-1.2,2-trifiuoroethane (1) forms l,l,1.2-tetrachloro-2,2-difluoroethane (2) and... 

Carbide Aluminum carbide A14C3, yellowish-green solid, by reaction of aluminum oxide and carbon in the electric furnace, reacts with H.O to yield methane gas and aluminum hydroxide. 

Further Reduction to a Hydrocarbon. In the reduction of benzo-phenone with aluminum ethoxide the formation of 7% of diphenyl-methane was observed. When benzohydrol was treated with aluminum ethoxide under the same conditions, 28% reduction to diphenylmethane occurred.12 In these reactions acetic acid, rather than acetaldehyde,-was formed from the ethoxide. Aluminum isopropoxide does not give this type of undesirable reaction with this reagent, pure benzohydrol is easily obtained in 100% yield from benzophenone.6 37 However, one case of reduction of a ketone to the hydrocarbon has been observed with aluminum isopropoxide.17 When 9, 9-dimethylanthrone-10 (XU) was reduced in xylene solution, rather than in isopropyl alcohol, to avoid formation of the ether (see p. 190), the hydrocarbon XUII was formed in 65% yield. The reduction in either xylene or isopropyl alcohol was very slow, requiring two days for completion. 

Tellurols, derivatives of dihydrogen telluride, have received little attention. Only methane-, ethane-, propane-, and butane tellur ol have been isolated from reactions of aluminum telluride with alcohols at 300° or from additions of alkyl bromides to a solution of dihydrogen telluride in absolute ethanol containing sodium ethoxide (s. Vol. IX, 970). No arenetellurol has yet been isolated. 

Ignition or explosive reaction with metals (e.g., aluminum, antimony powder, bismuth powder, brass, calcium powder, copper, germanium, iron, manganese, potassium, tin, vanadium powder). Reaction with some metals requires moist CI2 or heat. Ignites with diethyl zinc (on contact), polyisobutylene (at 130°), metal acetylides, metal carbides, metal hydrides (e.g., potassium hydride, sodium hydride, copper hydride), metal phosphides (e.g., copper(II) phosphide), methane + oxygen, hydrazine, hydroxylamine, calcium nitride, nonmetals (e.g., boron, active carbon, silicon, phosphoms), nonmetal hydrides (e.g., arsine, phosphine, silane), steel (above 200° or as low as 50° when impurities are present), sulfides (e.g., arsenic disulfide, boron trisulfide, mercuric sulfide), trialkyl boranes. 

Pertritiated methane (produced by the reaction of aluminum carbide with T2O) yields tritiated methyl cations (symbolized as CTj"), whose gas phase chemistry has been extensively studied by Nefedov s group in Russia. One of their first major contributions was to provide evidence for methyl migration around protonated benzene rings, as summarized in Table In mixtures of xylenes (at their vapor pressure) and pertritiated methane,... 

CHLOR-METHAN (German) (74-87-3) Flammable gas (flash point <32°F/<0°C). Moisture causes decomposition. Violent reaction with strong oxidizers, acetylene, anhydrous ammonia, amines, fluorine, interhalogens, magnesium, potassium, sodium, zinc, and their alloys. Reacts with barium, lithium, titanium. Contact with powdered aluminum or aluminum chloride forms pyrophoric trimethylaluminum may cause ignition or explosion. Attacks plastics, rubber, and coatings. 

METHANE TETRABROMHJE (558-13-4) Violent reaction with fluorine, hexylcyclo-hexyldilead, oxygen, potassium, potassium acetylene-1,2-dioxide, sodium azide, uranium(III) hydride. Mixtures with finely divided aluminum, lithium, magnesium, potassium-sodium alloy, titanium, zinc can form a friction- or shock-sensitive explosive material. Incompatible with decaborane. Attacks active metals. 

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