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・ Phenylethanoid
・ Phenylethanolamine
・ Phenylethanolamine N-methyltransferase
・ Phenylethylidenehydrazine
・ Phenylethylmalonamide
・ Phenylethylpyrrolidine
・ Phenylglyoxal
・ Phenylglyoxylate dehydrogenase (acylating)
・ Phenylglyoxylic acid
・ Phenylhydrazine
・ Phenylhydroxylamine
・ Phenylisobutylamine
・ Phenylisocyanate
・ Phenylketonuria
・ Phenyllithium
Phenylmagnesium bromide
・ Phenylmercuric borate
・ Phenylmercury acetate
・ Phenylobacterium immobile
・ Phenylphosphine
・ Phenylpiperazine
・ Phenylpiperidine
・ Phenylpropanoic acid
・ Phenylpropanoid
・ Phenylpropanoids metabolism
・ Phenylpropanolamine
・ Phenylpropene
・ Phenylpropiolic acid
・ Phenylpropylaminopentane
・ Phenylpyruvate decarboxylase


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Phenylmagnesium bromide : ウィキペディア英語版
Phenylmagnesium bromide

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Phenylmagnesium bromide, with the simplified formula , is a magnesium-containing organometallic compound. It is commercially available as a solution in diethyl ether or tetrahydrofuran (THF). Phenylmagnesium bromide is a Grignard reagent. It is often used as a synthetic equivalent for the phenyl "Ph" synthon.
==Preparation==

Phenylmagnesium bromide is commercially available as solutions of diethyl ether or THF. Laboratory Preparation involves treating bromobenzene with magnesium metal, usually in the form of turnings. A small amount of iodine may be used to activate the magnesium to initiate the reaction.
Coordinating solvents such as ether or THF, are required to solvate (complex) the magnesium(II) center. The solvent must be aprotic since alcohols and water contain an acidic proton and thus react with phenylmagnesium bromide to give benzene. Carbonyl-containing solvents, such as acetone and ethyl acetate, are also incompatible with the reagent.

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