• 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...
    16 KB (1,804 words) - 21:38, 3 June 2024
  • 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...
    48 KB (5,450 words) - 14:18, 26 September 2024
  • Thumbnail for Ether
    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...
    19 KB (1,835 words) - 18:47, 14 October 2024
  • 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...
    25 KB (3,056 words) - 03:04, 30 March 2022
  • Thumbnail for Amine
    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...
    36 KB (3,789 words) - 11:52, 8 November 2024
  • Thumbnail for Haloalkane
    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...
    20 KB (2,413 words) - 06:14, 8 September 2024
  • The Wurtz–Fittig reaction is the chemical reaction of an aryl halide, alkyl halides, and sodium metal to give substituted aromatic compounds. Following...
    9 KB (915 words) - 00:40, 20 November 2023
  • bonds via the palladium-catalyzed coupling reactions of amines with aryl halides. Although Pd-catalyzed C–N couplings were reported as early as 1983,...
    31 KB (3,483 words) - 01:36, 25 April 2024
  • Thumbnail for Grignard reagent
    reagent would attack the ester group over the aryl halide. For the coupling of aryl halides with aryl Grignard reagents, nickel chloride in tetrahydrofuran...
    24 KB (2,752 words) - 01:37, 23 October 2024
  • 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...
    34 KB (3,845 words) - 17:47, 26 September 2024
  • 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...
    5 KB (433 words) - 23:41, 31 January 2024
  • reaction is the copper-promoted conversion of aryl halides to aryl ethers, aryl thioethers, aryl nitriles, and aryl amines. These reactions are examples of...
    7 KB (800 words) - 23:53, 31 August 2024
  • Thumbnail for Michaelis–Arbuzov reaction
    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...
    13 KB (1,591 words) - 16:54, 5 November 2024
  • The Sandmeyer reaction is a chemical reaction used to synthesize aryl halides from aryl diazonium salts using copper salts as reagents or catalysts. It...
    16 KB (1,738 words) - 18:24, 22 October 2024
  • 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...
    4 KB (454 words) - 19:31, 27 October 2022
  • 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...
    3 KB (290 words) - 03:56, 9 July 2022
  • to achieve high selectivity for cross product. For example, aryl halide and alkyl halide can be differentiated by the reactivity trends of two electrophiles...
    6 KB (698 words) - 15:18, 22 June 2024
  • exchange is frequently used to prepare vinyl-, aryl- and primary alkyllithium reagents. Vinyl halides usually undergo lithium–halogen exchange with retention...
    10 KB (1,200 words) - 17:34, 25 September 2023
  • Thumbnail for Rosenmund–von Braun reaction
    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...
    3 KB (337 words) - 22:27, 27 September 2024
  • Thumbnail for XPhos
    involving aryl chlorides and aryl tosylates. Both palladium and copper complexes of the compound exhibit high activity for the coupling of aryl halides and...
    5 KB (359 words) - 14:46, 5 March 2024
  • Thumbnail for 1-Bromo-4-iodobenzene
    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...
    4 KB (279 words) - 17:20, 21 March 2024
  • Thumbnail for Organocopper chemistry
    retention of subtrate’s configuration. Organocopper compounds couple with aryl halides (see Ullmann condensation and Ullmann reaction): ArX + ( Ar ′ ) 2 CuLi...
    23 KB (2,441 words) - 02:00, 1 August 2024
  • 2-dichloroethane. Traditionally, aryl amination is difficult reaction which usually requires "activated" aryl halides, such as those with strong electron-withdrawing...
    6 KB (814 words) - 00:53, 9 July 2022
  • to slow reactions. The organic residue R = alkenyl, aryl, allyl, alkynyl or propargyl. The halide X' in the organozinc compound can be chloride, bromine...
    34 KB (3,954 words) - 20:12, 15 June 2024
  • 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...
    13 KB (1,355 words) - 19:29, 15 December 2023
  • introduced. The classical Ullmann reaction is limited to electron deficient aryl halides (hence the example of 2-nitrophenyl chloride above) and requires harsh...
    15 KB (1,600 words) - 19:18, 5 November 2024
  • Thumbnail for Mesityl bromide
    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...
    2 KB (140 words) - 23:10, 28 December 2023
  • Bromochlorobenzenes are mixed aryl halides (aryl chloride and aryl bromide) consisting bromine and chlorine as substituents on a benzene ring. All three...
    5 KB (268 words) - 03:11, 12 February 2024
  • Thumbnail for Alkylation
    can displace halide substituents on a carbon atom through the SN2 mechanism. With a catalyst, they also alkylate alkyl and aryl halides, as exemplified...
    15 KB (1,651 words) - 13:59, 24 August 2024
  • {\color {Red}{\ce {R^2}}}} : Allyl, alkenyl, aryl, benzyl, acyl X {\displaystyle {\color {Red}{\ce {X}}}} : halides (Cl, Br, I), pseudohalides (OTf, OPO(OR)2)...
    47 KB (5,491 words) - 13:23, 22 February 2024