Anilide

General structure of an anilide, where R denotes possible substituents

In organic chemistry, anilides (or phenylamides) are a class of organic compounds with the general structure R−C(=O)−N(−R’)−C₆H₅. They are amide derivatives of aniline (H₂N−C₆H₅).

Preparation

Aniline reacts with acyl chlorides or 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.

Uses

• Herbicides - diflufenican, dimethenamid, flamprop, propanil, tetflupyrolimet, acetochlor, alachlor, butachlor, delachlor, diethatyl, dimethachlor, ethaprochlor, metazachlor, pretilachlor, propisochlor, pyrnachlor, terbuchlor, thenylchlor, xylachlor
• Fungicides - Oxycarboxin, Carboxin

External links

• Media related to Anilides at Wikimedia Commons