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  2. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    An industrial synthesis of paracetamol developed by Hoechst–Celanese involves the conversion of a methyl ketone to an acetanilide via a Beckmann rearrangement. [15] The thermal rearrangement that occurs in the synthesis of ketamine was claimed to be a Beckmann rearrangement according to: url.

  3. Acetanilide - Wikipedia

    en.wikipedia.org/wiki/Acetanilide

    Acetanilide can be produced by reacting acetic anhydride with aniline: [7]. C 6 H 5 NH 2 + (CH 3 CO) 2 O → C 6 H 5 NHCOCH 3 + CH 3 COOH. The preparation used to be a traditional experiment in introductory organic chemistry lab classes, [8] but it has now been widely replaced by the preparation of either paracetamol or aspirin, both of which teach the same practical techniques (especially ...

  4. Phenacetin - Wikipedia

    en.wikipedia.org/wiki/Phenacetin

    Morse's cited article describes the synthesis of paracetamol from 4-aminophenol and acetic acid. [6] Phenacetin may be synthesized as an example of the Williamson ether synthesis: ethyl iodide, paracetamol, and anhydrous potassium carbonate are heated in 2-butanone to give the crude product, which is recrystallized from water. [7]

  5. Anilide - Wikipedia

    en.wikipedia.org/wiki/Anilide

    For example, reaction of aniline with acetyl chloride provides acetanilide (CH 3 −CO−NH−C 6 H 5). At high temperatures, aniline and carboxylic acids react to give anilides. At high temperatures, aniline and carboxylic acids react to give anilides.

  6. Fries rearrangement - Wikipedia

    en.wikipedia.org/wiki/Fries_rearrangement

    Therefore, this reaction is of industrial importance for the synthesis of hydroxyarylketones, which are important intermediates for several pharmaceuticals. As an alternative to aluminium chloride , other Lewis acids such as boron trifluoride and bismuth triflate or strong protic acids such as hydrogen fluoride and methanesulfonic acid can also ...

  7. Category:Acetanilides - Wikipedia

    en.wikipedia.org/wiki/Category:Acetanilides

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  8. 4-Aminoacetanilide - Wikipedia

    en.wikipedia.org/wiki/4-aminoacetanilide

    4-Aminoacetanilide or paracetamin is a chemical compound which is a amino derivative of acetanilide and para-isomer of aminoacetanilide. There are two other isomers of aminoacetanilide, 2-aminoacetanilide and 3-aminoacetanilide. Aminoacetanilide derivatives are important synthetic intermediates in heterocyclic and aromatic synthesis. These ...

  9. Acetylation - Wikipedia

    en.wikipedia.org/wiki/Acetylation

    Salicylic acid is acetylated to form aspirin. In chemistry, acetylation is an organic esterification reaction with acetic acid.It introduces an acetyl group into a chemical compound.