Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Magnesium, organo- compounds reaction

Anhydrous diethyl ether is the customary solvent used when preparing organo magnesium compounds Sometimes the reaction does not begin readily but once started It IS exothermic and maintains the temperature of the reaction mixture at the boiling point of diethyl ether (35°C)... [Pg.591]

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]

A Polymeride of Cyclopentamethylenesilicone is isolated by the following reactions Cyclopentamethylenesilicon dichloride is obtained by the action of the organo-magnesium compound derived from 1 5 dibromopentane on silicon tetrachloride in ethereal solution. Cyclopentamethylenesilicon dichloride,... [Pg.282]


See other pages where Magnesium, organo- compounds reaction is mentioned: [Pg.744]    [Pg.11]    [Pg.102]    [Pg.131]    [Pg.416]    [Pg.162]    [Pg.243]    [Pg.662]    [Pg.444]    [Pg.339]    [Pg.32]    [Pg.200]    [Pg.572]    [Pg.211]    [Pg.331]    [Pg.118]    [Pg.169]    [Pg.700]    [Pg.713]    [Pg.417]    [Pg.109]    [Pg.279]    [Pg.8]    [Pg.10]    [Pg.34]    [Pg.102]    [Pg.355]    [Pg.765]    [Pg.40]    [Pg.40]    [Pg.292]    [Pg.443]    [Pg.12]    [Pg.279]    [Pg.279]    [Pg.209]    [Pg.226]    [Pg.461]    [Pg.29]    [Pg.8]   
See also in sourсe #XX -- [ Pg.634 , Pg.635 , Pg.636 , Pg.637 , Pg.638 , Pg.639 , Pg.640 , Pg.641 , Pg.642 , Pg.643 ]




SEARCH



Magnesium compounds

Magnesium compounds reactions

Magnesium reactions

Magnesium, organo- compounds

Magnesium, organo- compounds reactions with

Organo compounds

Organo magnesium

© 2024 chempedia.info