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Grignard reagents or Grignard compounds are chemical compounds with the general formula R−Mg−X, where X is a halogen and R is an organic group, normally an alkyl or aryl. Two typical examples are methylmagnesium chloride Cl−Mg−CH 3 and phenylmagnesium bromide (C 6 H 5 )−Mg−Br .
A solution of a carbonyl compound is added to a Grignard reagent. (See gallery) An example of a Grignard reaction (R 2 or R 3 could be hydrogen). The Grignard reaction (French:) is an organometallic chemical reaction in which, according to the classical definition, carbon alkyl, allyl, vinyl, or aryl magnesium halides (Grignard reagent) are added to the carbonyl groups of either an aldehyde or ...
The reaction is named after pinacol (also known as 2,3-dimethyl-2,3-butanediol or tetramethylethylene glycol), which is the product of this reaction when done with acetone as reagent. The reaction is usually a homocoupling but intramolecular cross-coupling reactions are also possible. Pinacol was discovered by Wilhelm Rudolph Fittig in 1859
Aluminum amalgam (Al/Hg) may be used for the chemoselective reduction of α-sulfonylated carbonyl groups. Carboxylic acid derivatives, acetals, thioacetals, amines, alcohols, and isolated double bonds are all inert to Al/Hg. Selective desulfonylation may be carried out on β-hydroxy sulfones without reductive elimination.
Mercury(II) acetate, also known as mercuric acetate is a chemical compound, the mercury(II) salt of acetic acid, with the formula Hg(O 2 CCH 3) 2. Commonly abbreviated Hg(OAc) 2, this compound is employed as a reagent to generate organomercury compounds from unsaturated organic precursors. It is a white, water-soluble solid, but some samples ...
The Hg(SCN) 3− ion can also exist independently and is easily generated from the compounds above, amongst others. [5] Organic halides attack Hg(SCN) 2 to give a mercuric halide and a mixture of the corresponding thiocyanate and isothiocyanate. [6] Mercuric thiocyanate catalyzes HSCN or BrSCN addition (either reagent formed in situ) to alkynes ...
Mercury(I) nitrate is an inorganic compound, a salt of mercury and nitric acid with the formula Hg 2 (NO 3) 2. A yellow solid, the compound is used as a precursor to other Hg 2 2+ complexes. The structure of the hydrate has been determined by X-ray crystallography. It consists of a [H 2 O-Hg-Hg-OH 2] 2+ center, with a Hg-Hg distance of 254 pm. [2]
Organomercury compounds are versatile synthetic intermediates due to the well controlled conditions under which they undergo cleavage of the Hg-C bonds. Diphenylmercury is a source of the phenyl radical in certain syntheses. Treatment with aluminium gives triphenyl aluminium: 3 Ph 2 Hg + 2 Al → (AlPh 3) 2 + 3 Hg