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Magnesium, organo- compounds reactions with

Coupling of acetylenes and halides, copper-promoted, 50,100 Cuprous chloride, reaction with an organo-magnesium compound, 50,98... [Pg.77]

In its action on organo-magnesium compounds,3 sulphur tetrachloride behaves as if it consists only of sulphur dichloride and chlorine, and its reactions with sulphur trioxide (see before) appear to be capable of a similar interpretation in these cases it is indeed possible that sulphur dichloride and chlorine, present as products of dissociation, are the actual agents in the chemical change. [Pg.83]

Aminomethylotion. The reagent reacts with Grignard reagents to form N,N-bis(trimethylsilyl)amines in 60-90% yield (equation I). A similar reaction with organo-lithium compounds requires added magnesium biomide for satisfactory yields. ... [Pg.62]

Organo Vinyl Tellurium (from Vinyl Tellurium Iodides) A solution of the vinyl tellurium iodide, prepared by addition of 0.25 g (1.0 mmol) iodine in benzene to the divinyl ditelluride (1.0 mmol) in 5 ml tetrahydrofuran at 0° under nitrogen, is added dropwise to a solution of the organo magnesium bromide in 10 m/ tetrahydrofuran at 0°. The mixture is stirred at 20° for 1 h, hydrolyzed with a saturated aqueous solution of ammonium chloride, extracted with diethyl ether, the extract dried with magnesium sulfate and evaporated. The product is chromatographed on silica gel with petroleum ether (30-60°)/ethyl acetate (9 1) as eluent. The following compounds were prepared in this manner (yields in parentheses are for the reactions with vinyl tellurium iodides) ... [Pg.417]

Lead salts of other inorganic and of organic acids may replace the lead chloride, as also may lead oxide or sulfide, and these may be brought into reaction with organo-lithium, -magnesium, -zinc, or -aluminum compounds methods for obtaining tetraethyllead have been studied in particular detail.465... [Pg.803]

Reaction with Organometallic Compounds. Organo-magnesium (eq 4), lithium, and other main group metals readily undergo ligand transfer with PCI3 to form mono-, di-, or trialkyl(aryl) phosphines. A subclass of reactions include Aluminum Chloride-assisted transformations to form phosphetanes (eq 5). ... [Pg.334]


See other pages where Magnesium, organo- compounds reactions with is mentioned: [Pg.162]    [Pg.211]    [Pg.744]    [Pg.417]    [Pg.10]    [Pg.765]    [Pg.11]    [Pg.443]    [Pg.29]    [Pg.37]    [Pg.443]    [Pg.194]    [Pg.11]    [Pg.15]    [Pg.102]    [Pg.131]    [Pg.416]    [Pg.662]    [Pg.444]    [Pg.339]    [Pg.32]    [Pg.200]    [Pg.572]    [Pg.331]    [Pg.118]    [Pg.169]    [Pg.713]    [Pg.109]    [Pg.279]    [Pg.355]    [Pg.40]    [Pg.40]    [Pg.292]    [Pg.12]    [Pg.279]    [Pg.279]    [Pg.209]    [Pg.226]    [Pg.461]    [Pg.800]    [Pg.436]   


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Magnesium compounds

Magnesium compounds reactions

Magnesium reactions

Magnesium reactions with

Magnesium, organo- compounds

Magnesium, organo- compounds reaction

Organo compounds

Organo magnesium

Organo reactions with

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