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  2. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/FriedelCrafts_reaction

    The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring. [1] Friedel–Crafts reactions are of two main types: alkylation reactions and acylation reactions. Both proceed by electrophilic aromatic substitution. [2] [3] [4] [5]

  3. Electrophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    This reaction is typically catalyzed by the corresponding iron or aluminum trihalide. The Friedel–Crafts reaction can be performed either as an acylation or as an alkylation. Often, aluminium trichloride is used, but almost any strong Lewis acid can be applied. For the acylation reaction a stoichiometric amount of aluminum trichloride is ...

  4. Electrophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_substitution

    In electrophilic substitution in aromatic compounds, an atom appended to the aromatic ring, usually hydrogen, is replaced by an electrophile.The most important reactions of this type that take place are aromatic nitration, aromatic halogenation, aromatic sulfonation and acylation and alkylating Friedel-Crafts reactions.

  5. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Baeyer–Villiger oxidation, Baeyer–Villiger rearrangement [12] Bakeland process (Bakelite) ... Freund reaction; Friedel–Crafts acylation; Friedel–Crafts ...

  6. Adamantane - Wikipedia

    en.wikipedia.org/wiki/Adamantane

    Adamantane interacts with benzene in the presence of Lewis acids, resulting in a Friedel–Crafts reaction. [47] Aryl-substituted adamantane derivatives can be easily obtained starting from 1-hydroxyadamantane. In particular, the reaction with anisole proceeds under normal conditions and does not require a catalyst. [41]

  7. Stollé synthesis - Wikipedia

    en.wikipedia.org/wiki/Stollé_synthesis

    The Stollé synthesis is a series of chemical reactions that produce oxindoles from ... while the second step is a Friedel–Crafts reaction. [5] [6] An improved ...

  8. Phenethyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_alcohol

    Phenethyl alcohol is prepared commercially via two routes. Most common is the Friedel-Crafts reaction between benzene and ethylene oxide in the presence of aluminium trichloride. C 6 H 6 + CH 2 CH 2 O + AlCl 3 → C 6 H 5 CH 2 CH 2 OAlCl 2 + HCl. The reaction affords the aluminium alkoxide that is subsequently hydrolyzed to the desired product.

  9. Charles Friedel - Wikipedia

    en.wikipedia.org/wiki/Charles_Friedel

    A native of Strasbourg, France, he was a student of Louis Pasteur at the Sorbonne.In 1876, he became a professor of chemistry and mineralogy at the Sorbonne.. Friedel developed the Friedel-Crafts alkylation and acylation reactions with James Crafts in 1877, [2] [3] and attempted to make synthetic diamonds.