Halides organomagnesiums

Grignard reagent (Section 14 4) An organomagnesium com pound of the type RMgX formed by the reaction of magne Slum with an alkyl or aryl halide... 

Reactions of Enamine Salts with OrganometalUc Compounds Organolithium and organomagnesium compounds react with enamine salts to give amines substituted on the ix-carbon atoms. The treatment of. -dehydroquinolizidinium perchlorate (163) with alkylmagnesium halides gives 9-alkylated quinolizidines (164) (252,256). Formation of... 

Oddo reported that the organomagnesium derivatives of p3Trole, indole, skatole, and carbazole could be prepared in a single operation by mixing the parent heterocyclic compound with an alkyl halide and magnesium in anhydrous ether.The product formed was reported to be the same as that obtained by the more conventional procedure. However, this approach to the synthesis of the indole Grignard reagents does not seem to have been exploited in subsequent work. 

The much simpler steroid, 253, was fortuitously found to fulfill this role when injected into animals. Its lack of oral activity was overcome by incorporation of the 7a-thioacetate group. Reaction of the ethisterone intermediate, 77b, with a large excess of an organomagnesium halide leads to the corresponding acetylide salt carbonation with CO2 affords the carboxyllic acid, 251. This is then hydrogenated and the hydroxy acid cy-clized to the spirolactone. Oppenauer oxidation followed by treatment with chloranil affords the 4,6-dehydro-3-ketone (254). Conjugate addition of thiolacetic acid completes the synthesis of spironolactone (255), an orally active aldosterone antagonist. ... 

The reduction of carbonyl compounds by reaction with hydride reagents (H -) and the Grignard addition by reaction with organomagnesium halides (R - +MgBr) are examples of nucleophilic carbonyl addition reactions. What analogous product do you think might result from reaction of cyanide ion with a ketone ... 

Grignard reagent (Section 10.7) An organomagnesium halide, RMgX. 

As precursors of the organocopper compounds, organolithium reagents are slightly preferable to organomagnesium halides. 

Allenyl and 1- and 2-alkynyl sulfoxides have also been prepared by reaction of organomagnesium halides with sulfinate ester 19. 1-Alkynyl p-tolyl sulfoxides were prepared in good yield from 1-alkynylmagnesium halides plus ester 19 in toluene (equation ll)63. The corresponding organolithium compound was unsatisfactory as a... 

Organomagnesium halide reagents RMgX (RX = CjH,Br, i-PrBr, n-BuBr, PhBr) react in toluene-ether with (t7 -Cp)2MoH2 to form compounds II, in which each molecule contains four Mo—Mg bonds " . When II is dissolved in THF a red solution is formed, which after concentration yields orange crystals of III. Compound III is monomeric with a Mo—Mg bond of length 273.2 pm, consistent for Mo as a one-electron donor. 

The position of the equilibrium depends upon the solvent and the identity of the specific organic group, but in ether lies well to the left for simple aryl-, alkyl-, and alkenylmagnesium halides.21 Solutions of organomagnesium compounds in diethyl ether contain aggregated species.22 Dimers predominate in ether solutions of alkylmagnesium chlorides. 

Organomagnesium halides were discovered by the French chemist Victor Grignard in 1900. 

Grignard received the Nobel Prize in 1912 and organomagnesium halides are now called Grignard reagents. 

The order of reactivity of halides with magnesium is RI > RBr > RC1 (very few organomagnesium fluorides have been prepared), i) Aryl Grignard reagents are more easily prepared from aryl bromides and aryl iodides than from aryl chlorides, which react very sluggishly. 

Addition of an excess of organolithium or organomagnesium reagents to germanium halides results in the deplacement of the halide ions and the formation of tetra-alkyl and -arylgermanium compounds. Representative examples of these reactions are shown in equations 4 and 5, respectively. 

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