In organic chemistry, an aryl halide (also known as haloarene) is an aromatic compound in which one or more hydrogen atoms, directly bonded to an aromatic...
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form a carbon–carbon bond between a terminal alkyne and an aryl or vinyl halide. R1: aryl or vinyl R2: arbitrary X: I, Br, Cl or OTf The Sonogashira cross-coupling...
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Ether (redirect from Aryl ether)
well for aryl halides (e.g. bromobenzene, see Ullmann condensation below). Likewise, this method only gives the best yields for primary halides. Secondary...
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Decarboxylative cross-coupling (section Aryl alkynes)
is reacted with an organic halide to form a new carbon-carbon bond, concomitant with loss of CO2. Aryl and alkyl halides participate. Metal catalyst...
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Haloalkane (redirect from Alkyl halide)
a comparatively easy method to make aryl halides as the gaseous product can be separated easily from aryl halide. When an iodide is to be made, copper...
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Amine (section From alkyl and aryl halides)
phthalimide. Aryl halides are much less reactive toward amines and for that reason are more controllable. A popular way to prepare aryl amines is the...
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bonds via the palladium-catalyzed coupling reactions of amines with aryl halides. Although Pd-catalyzed C–N couplings were reported as early as 1983,...
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The Wurtz–Fittig reaction is the chemical reaction of an aryl halide, alkyl halides, and sodium metal to give substituted aromatic compounds. Following...
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Grignard reagent (redirect from Organomagnesium halide)
reagent would attack the ester group over the aryl halide. For the coupling of aryl halides with aryl Grignard reagents, nickel chloride in tetrahydrofuran...
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reagents can be used for the Suzuki coupling, e.g., aryl or vinyl boronic acids and aryl or vinyl halides. Work has also extended the scope of the reaction...
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between a copper(I) acetylide and an aryl halide in pyridine, forming a disubstituted alkyne and a copper(I) halide. The reaction was described in 1963...
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reaction is the copper-promoted conversion of aryl halides to aryl ethers, aryl thioethers, aryl nitriles, and aryl amines. These reactions are examples of...
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Michaelis–Arbuzov reaction (section Alkyl halide)
alkyl halides, aryl halides and vinyl halides do not react. There are notable exceptions to this trend, including 1,2-dichloroethene and trityl halides. Some...
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The Sandmeyer reaction is a chemical reaction used to synthesize aryl halides from aryl diazonium salts using copper salts as reagents or catalysts. It...
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Braun synthesis is an organic reaction in which an aryl halide reacts with cuprous cyanide to yield an aryl nitrile. The reaction was named after Karl Wilhelm...
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reaction that replaces an alkyl or aryl halide with a formyl group using a N,N-disubstituted formamide. For primary alkyl halides this produces the homologous...
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aryl halide 1 accepts an electron from a radical initiator forming a radical anion 2. This intermediate collapses into an aryl radical 3 and a halide...
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1-Bromo-4-iodobenzene is a mixed aryl halide (aryl bromide and aryl iodide) with the formula BrC6H4I. In one laboratory route to 1-bromo-4-iodobenzene...
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involving aryl chlorides and aryl tosylates. Both palladium and copper complexes of the compound exhibit high activity for the coupling of aryl halides and...
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to achieve high selectivity for cross product. For example, aryl halide and alkyl halide can be differentiated by the reactivity trends of two electrophiles...
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retention of subtrate’s configuration. Organocopper compounds couple with aryl halides (see Ullmann condensation and Ullmann reaction): ArX + ( Ar ′ ) 2 CuLi...
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carbonate, and sodium acetate. The aryl electrophile can be a halide (Br, Cl) or a triflate as well as benzyl or vinyl halides. The alkene must contain at least...
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2-dichloroethane. Traditionally, aryl amination is difficult reaction which usually requires "activated" aryl halides, such as those with strong electron-withdrawing...
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exchange is frequently used to prepare vinyl-, aryl- and primary alkyllithium reagents. Vinyl halides usually undergo lithium–halogen exchange with retention...
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to slow reactions. The organic residue R = alkenyl, aryl, allyl, alkynyl or propargyl. The halide X' in the organozinc compound can be chloride, bromine...
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Bromochlorobenzenes are mixed aryl halides (aryl chloride and aryl bromide) consisting bromine and chlorine as substituents on a benzene ring. All three...
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solvent. Aryl methane-sulfonates are deprotected and then followed by a nucleophilic aromatic substitution (SNAr) with activated aryl halides. As a base...
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introduced. The classical Ullmann reaction is limited to electron deficient aryl halides (hence the example of 2-nitrophenyl chloride above) and requires harsh...
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4-Fluorobromobenzene is a mixed aryl halide (aryl fluoride and aryl bromide) with the formula C6H4BrF. It is a derivative of benzene, with a bromine atom...
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Br. The compound is a colorless oil. It is a standard electron-rich aryl halide substrate for cross coupling reactions. With magnesium it reacts to give...
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