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Grignard reagent metal halide reaction with

Grignard reagents, organomagnesium halides, are prepared by the reaction of metallic magnesium with a wide range of organic halides (reaction 9.3). Dry ether type solvents are essential. [Pg.355]

Many organic halides do not react satisfactorily with lithium to form RLi ecMnpounds or with metallic magnesium to form Grignard reagents. The desired organolithium compound can often be prepared by a halogen-metal interconversion reaction ... [Pg.929]

Grignard reagents are prepared from organic halides by reaction with magnesium a Group II metal... [Pg.591]

Pyrroles do not react with alkyl halides in a simple fashion polyalkylated products are obtained from reaction with methyl iodide at elevated temperatures and also from the more reactive allyl and benzyl halides under milder conditions in the presence of weak bases. Alkylation of pyrrole Grignard reagents gives mainly 2-alkylated pyrroles whereas N-alkylated pyrroles are obtained by alkylation of pyrrole alkali-metal salts in ionizing solvents. [Pg.53]

Many other kinds of organometallic compounds can be prepared in a manner similar to that of Grignard reagents. For instance, alkyllithium reagents, RLi, can be prepared by the reaction of an alkyl halide with lithium metal. Alkyllithiums are both nucleophiles and strong bases, and their chemistry is similar in many respects to that of alkylmagnesium halides. [Pg.346]

Among others, alkyls of Be, Cd, Hg, Al, Sn, Pb, Co, Pt, and Au have been prepared by treatment of Grignard reagents with the appropriate halide. The reaction has been used to prepare alkyls of almost all non-transition metals and even of some transition metals. Alkyls of metalloids and of nonmetals, including Si,... [Pg.803]

Next to the formation of Grignard reagents, the most important application of this reaction is the conversion of alkyl and aryl halides to organolithium compounds, but it has also been carried out with many other metals, (e.g., Na, Be, Zn, Hg, As, Sb, and Sn). With sodium, the Wurtz reaction (10-93) is an important side reaction. In some cases, where the reaction between a halide and a metal is too slow, an alloy of the metal with potassium or sodium can be used instead. The most important example is the preparation of tetraethyl lead from ethyl bromide and a Pb—Na alloy. [Pg.806]


See other pages where Grignard reagent metal halide reaction with is mentioned: [Pg.15]    [Pg.397]    [Pg.8]    [Pg.230]    [Pg.644]    [Pg.849]    [Pg.148]    [Pg.180]    [Pg.131]    [Pg.951]    [Pg.58]    [Pg.73]    [Pg.653]    [Pg.188]    [Pg.183]    [Pg.214]    [Pg.20]    [Pg.400]    [Pg.16]    [Pg.206]    [Pg.240]    [Pg.314]    [Pg.1274]    [Pg.398]    [Pg.750]    [Pg.215]    [Pg.256]    [Pg.31]    [Pg.287]    [Pg.205]    [Pg.196]    [Pg.142]    [Pg.763]    [Pg.467]    [Pg.535]    [Pg.538]    [Pg.566]    [Pg.567]    [Pg.794]    [Pg.805]   
See also in sourсe #XX -- [ Pg.398 ]




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Grignard reagent metallation with

Grignard reagents reactions

Grignard reagents with halides

Grignard reagents with metal halides

Grignard with halides

Halides reagents

Metal halides reactions

Metal halides, reaction with

Metals Grignard reaction

Metals reactions with Grignard

Metals reagents

Reaction with Grignard reagents

With Grignard Reagents

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