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  2. Amidase - Wikipedia

    en.wikipedia.org/wiki/Amidase

    In enzymology, an amidase (EC 3.5.1.4, acylamidase, acylase (misleading), amidohydrolase (ambiguous), deaminase (ambiguous), fatty acylamidase, N-acetylaminohydrolase (ambiguous)) is an enzyme that catalyzes the hydrolysis of an amide. In this way, the two substrates of this enzyme are an amide and H 2 O, whereas its two products are ...

  3. Amide - Wikipedia

    en.wikipedia.org/wiki/Amide

    Mechanism for acid-mediated hydrolysis of an amide. [11] ... For N,N-diaryl amides. The reaction mechanism is based on a nucleophilic aromatic substitution. [26]

  4. Hydrolysis - Wikipedia

    en.wikipedia.org/wiki/Hydrolysis

    Mechanism for acid-catalyzed hydrolysis of an amide. Upon hydrolysis, an amide converts into a carboxylic acid and an amine or ammonia (which in the presence of acid are immediately converted to ammonium salts). One of the two oxygen groups on the carboxylic acid are derived from a water molecule and the amine (or ammonia) gains the hydrogen ion.

  5. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    In the third step, an isomerization step protonates the nitrogen atom leading to the amide. The Beckmann rearrangement mechanism. The same computation with a hydroxonium ion and 6 molecules of water has the same result, but when the migrating substituent is a phenyl group, the mechanism favors the formation of an intermediate three-membered π ...

  6. Madelung synthesis - Wikipedia

    en.wikipedia.org/wiki/Madelung_synthesis

    Next, the carbanion resulting from the benzylic hydrogen extraction performs a nucleophilic attack on the electrophilic carbonyl carbon of the amide group. When this occurs, the pi-bond of the amide is converted into a lone pair, creating a negatively charged oxygen. After these initial steps, strong base is no longer required and hydrolysis ...

  7. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    The Hofmann rearrangement (Hofmann degradation) is the organic reaction of a primary amide to a primary amine with one less carbon atom. [1] [2] [3] The reaction involves oxidation of the nitrogen followed by rearrangement of the carbonyl and nitrogen to give an isocyanate intermediate.

  8. Carbodiimide - Wikipedia

    en.wikipedia.org/wiki/Carbodiimide

    The formation of an amide using a carbodiimide is a common reaction, but carries the risk of several side reactions. The acid 1 will react with the carbodiimide to produce the key intermediate: the O-acylisourea 2 , which can be viewed as a carboxylic ester with an activated leaving group.

  9. Weerman degradation - Wikipedia

    en.wikipedia.org/wiki/Weerman_degradation

    Weermann degradation mechanism of Hydroxy-Carbonsäureamide. At first the carbonic acid amide (1) reacts with the sodium hypochlorite. After the separation of water and chloride an amine with a free bond is built 2. The intermediate (3) is generated by rearrangement. In the next step a hydrolysis takes place.