Anilide

In

C₆H₅. They are amide derivatives of aniline

Preparation

Aniline reacts with

carboxylic 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

Herbicides^[2]
Fungicides - Oxycarboxin,^[3] Carboxin^[4]

References

^ 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.

External links

Media related to Anilides at Wikimedia Commons

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[1] Carl N. Webb (1941). "Benzanilide". Organic Syntheses; Collected Volumes, vol. 1, p. 82.

[2] "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-3] PubChem. "Oxycarboxin". PubChem. National Center for Biotechnology Information. Retrieved 2020-12-06.

[PubChem-carboxin-4] PubChem. "Carboxin". PubChem. National Center for Biotechnology Information. Retrieved 2020-12-06.

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