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Halogenation halogen-metal exchange

The metal-halogen exchange reaction is useful in the synthesis of numerous perfluoroalkylmagnesium halides, some of which are shown in Table 2... [Pg.653]

Although the metal-halogen exchange reaction is the preferred method of synthesis, the conventional Grignard synthesis through the reaction of a per-fluoroorgano halide and magnesium occasionally is still used [49, 50]... [Pg.653]

Table 2. Perfluoroalkylmagnesium Halides (RfMgX) Prepared by Metal-Halogen Exchange... Table 2. Perfluoroalkylmagnesium Halides (RfMgX) Prepared by Metal-Halogen Exchange...
Novel polyfluoroethyl Gngnard reagents containmg fluonne, chlorine, and bromine are prepared through the metal-halogen exchange reaction [46] (equation 20)... [Pg.656]

To avoid this competing reaction, the metal-halogen exchange is performed in diethyl ether with either secondary or tertiary butyllithium at -60 °C to give the trifluorovinyllithium compound in near quantitative yield [59],... [Pg.660]

Protection of primary aryl amines as the triazene is accomplished by diazotiza-tion of the amine followed by reaction with pyrrolidine in aq. KOH. This group is stable to metalation of the aromatic ring by metal halogen exchange. The amine is recovered by reductive cleavage with Ni-Al alloy (aq. KOH, rt, 37-68% yield). ... [Pg.597]

Reactivity and yields are greatly enhanced by the presence of 0.5-1% Na in the Li. The reaction is also generally available for the preparation of metal alkyls of the heavier Group 1 metals. Lithium aryls are best prepared by metal-halogen exchange using LiBu" and an aryl iodide, and transmetalation is the most convenient route to vinyl, allyl and other unsaturated derivatives ... [Pg.102]

Metal-halogen exchange of 10-bromo-5-ethyl-5//-dibenz[/>,/]azepinc (52) with butyllithium followed by quenching with acetone yields the propan-2-ol 53.214... [Pg.272]

One of the most direct routes to vinylsilanes uses vinyl halides as starting materials. Metal-halogen exchange, followed by electrophilic attack by TMSC1, can often provide the vinylsilane quickly and in good yield. As an added bonus, vinyl bromides have been shown (10, II) to proceed through this sequence with retention of double-bond stereochemistry. [Pg.101]

Helquist and coworkers60 have developed a six-membered ring annulation via a conjugate addition of aryllithium generated by metal-halogen exchange and subsequent intramolecular alkylation. This is illustrated in equation 71. [Pg.781]

McLafferty rearrangement 133, 163 Meisenheimer complexes 699, 702 Metal-chelated intermediates 838 Metal-halogen exchange 781, 784 Methionine, oxidation of 852-855 Methionine sulphone 853 Methionine sulphoxide 851-869 reduction of 1063 residues of... [Pg.1202]

Limitations common to both salt elimination methods 1 and 2 are (a) the required product may be difficult to separate from the alkali metal halide, (b) reactions are best carried out in the solvent (usually an ether) in which the initial alkali metal derivative is prepared, (c) difficulties may arise through metal-halogen exchange (207), and (d) the range of starting anions is limited [e.g., X3Si compounds are only readily formed when X = H or Ar,... [Pg.264]

The second cycloaddition substrate took to form of 91 (Scheme 1.9b), incorporating a vinyl sulfone dipolarophile. Beginning with cyano ketone 84, which was readily prepared from 1,5-dicyanopentane via a previously reported three-step sequence [45], condensation with thiophenol produced vinyl sulfide 85 in 84 % yield. Vinyl sulfide 85 underwent bromination in acetonitrile to afford bromo-vinyl sulfide 86 (86 %), which was then treated with isopropylmagnesium chloride [46] to effect metal-halogen exchange affording an intermediate vinyl magnesium bromide species. Subsequent alkylation with Mel in the presence of catalytic CuCN provided the alkylated vinyl sulfide 87 in 93 % yield. The nitrile within vinyl... [Pg.11]

A more general approach utilizes metal-halogen exchanges because of the ready availability of monobromocyclopropanes by either... [Pg.14]

A related series of reactions derives from dibromocarbene adducts of olefins as in Eq. 28 32,33). Metal-halogen exchange at very low temperature produces the... [Pg.26]

Metal-free initiators, 14 258-259 Metal fullerenes, 2 718-719 Metal-halogen exchange, in pyridine chemistry, 22 107-108 Metal hydrazides, 23 567 Metal hydrides, 23 611-613 amines by reduction, 2 493 hydrogen storage and, 23 851 nitriding, 27 206-207 storage of, 23 786... [Pg.566]


See other pages where Halogenation halogen-metal exchange is mentioned: [Pg.91]    [Pg.5]    [Pg.20]    [Pg.10]    [Pg.647]    [Pg.647]    [Pg.653]    [Pg.658]    [Pg.659]    [Pg.106]    [Pg.265]    [Pg.110]    [Pg.109]    [Pg.632]    [Pg.186]    [Pg.187]    [Pg.187]    [Pg.187]    [Pg.188]    [Pg.367]    [Pg.78]    [Pg.214]    [Pg.651]    [Pg.202]    [Pg.219]    [Pg.15]    [Pg.216]    [Pg.8]    [Pg.493]    [Pg.544]    [Pg.576]    [Pg.310]   


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3- Bromofuran, halogen-metal exchange

4 -Bromoimidazole, halogen-metal exchange

5- Bromopyrimidine halogen-metal exchange

5-Bromoindole, halogen metal exchange

Aryl bromides, halogen-metal exchange

Aryl chlorides, halogen-metal exchange

Aryl halides halogen-metal exchange with

Aryl halides halogen—metal exchange

Arynes halogen-metal exchange

By metal-halogen exchange

Exchange reactions halogen-metal

Halogen exchange

Halogen-Metal Exchange Relations

Halogen-metal exchange

Halogen-metal exchange reaction, acidic

Halogen-metal exchange reaction, acidic proton

Halogen-metal exchange reagents

Halogen-metal exchange reduction

Halogen-metal exchange stereochemistry

Halogen-metal exchange, and

Halogenation Metal-halogen exchange Quinoline

Intramolecular halogen-metal exchange

Isothiazoles halogen-metal exchange

Lithium, alkyl-: addn. to 1-alkenyl silanes halogen-metal exchange with

Metal-halogen

Metal-halogen exchange substitution reactions

Metal-halogen exchange synthesis

Metal-halogen exchange, with

Nucleophilic Substitution, Metallation, and Halogen-Metal Exchange

Organolithium reagents metal-halogen exchange

Organometallic compounds halogen-metal exchange reactions

Organometallics metal-halogen exchange

Pyrazole halogen-metal exchange

Thiophene metal-halogen exchange

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