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Contents

   



(Top)
 


1 Preparation  





2 Uses  





3 References  





4 External links  














Anilide






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From Wikipedia, the free encyclopedia
 


General structure of an anilide, where R denotes possible substituents

Inorganic chemistry, anilides (orphenylamides) are a class of organic compounds with the general structure R−C(=O)−N(−R’)−C6H5. They are amide derivativesofaniline (H2N−C6H5).

Preparation

[edit]

Aniline reacts with acyl chloridesorcarboxylic anhydrides to give anilides. For example, reaction of aniline with acetyl chloride provides acetanilide (CH3−CO−NH−C6H5). At high temperatures, aniline and carboxylic acids react to give anilides.[1]

Uses

[edit]

References

[edit]
  1. ^ Carl N. Webb (1941). "Benzanilide". Organic Syntheses; Collected Volumes, vol. 1, p. 82.
  • ^ "Anilide herbicides". Pesticide Target Interaction Database. East China University of Science & Technology. Archived from the original on 2018-06-24. Retrieved 2018-06-24.
  • ^ PubChem. "Oxycarboxin". PubChem. National Center for Biotechnology Information. Retrieved 2020-12-06.
  • ^ PubChem. "Carboxin". PubChem. National Center for Biotechnology Information. Retrieved 2020-12-06.
  • [edit]


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