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  2. 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 ...

  3. Anilide - Wikipedia

    en.wikipedia.org/wiki/Anilide

    Aniline reacts with acyl chlorides or carboxylic anhydrides to give anilides. 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.

  4. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    In organic chemistry, the Schmidt reaction is an organic reaction in which an azide reacts with a carbonyl derivative, usually an aldehyde, ketone, or carboxylic acid, under acidic conditions to give an amine or amide, with expulsion of nitrogen.

  5. Lumière–Barbier method - Wikipedia

    en.wikipedia.org/wiki/Lumière–Barbier_method

    Illustrative is the acetylation of aniline. First aniline is dissolved in water using one equivalent of hydrochloric acid. This solution is subsequently treated, sequentially, with acetic anhydride and aqueous sodium acetate. Aniline attacks acetic anhydride followed by deprotonation of the ammonium ion: Acetate then acts as a leaving group:

  6. Category:Acetanilides - Wikipedia

    en.wikipedia.org/wiki/Category:Acetanilides

    Download as PDF; Printable version; In other projects Wikimedia Commons; Wikidata item; ... Acetanilides are compounds based on acetanilide, or N-phenylacetamide.

  7. Acetoacetanilide - Wikipedia

    en.wikipedia.org/wiki/Acetoacetanilide

    It is the acetoacetamide derivative of aniline. It is a white solid that is poorly soluble in water. It is a white solid that is poorly soluble in water. This chemical and many related compounds (prepared from various aniline derivatives) are used in the production of organic pigments called arylide yellows , one example being Pigment Yellow 74 .