Acetanilide is a colourless, odourless solid compound that resembles a leaf or flake. It is also known as N-phenylacetamide, acetal, or acetanilid, and was previously known as Antifebrin. When aniline is heated in the presence of zinc dust and glacial acetic acid, it interacts with acetic anhydride to form acetanilide. As a result, the produced acetanilide is recrystallized to get pure crystals. The use of zinc dust is intended to avoid aniline oxidation during the process.
Acetanilide may be synthesized by combining acetic anhydride with aniline:
C6H5NH2 + (CH3CO)2O → C6H5NHCOCH3 + CH3COOH
The preparation used to be a standard experiment in introductory organic chemistry lab classes, but it has since been largely replaced by the preparation of either paracetamol or aspirin, both of which teach the same practical techniques (particularly recrystallization of the product) but avoid the use of aniline, a suspected carcinogen.
Acetanilide is used to stabilize cellulose ester varnishes and as a hydrogen peroxide breakdown inhibitor. It has also been used as an intermediator in the manufacture of rubber accelerators, colours and dye intermediates, and camphor. Acetanilide is used to make 4-acetamidobenzenesulfonyl chloride, a critical intermediary in the synthesis of sulfa medicines.
Acetanilide is a vital chemical molecule that is extensively employed in the pharmaceutical business. It is a white, odourless, solid, or flaky substance. Its preparation method is utilized in chemistry laboratories to teach students to organic compound synthesis.
Acetanilide dissolves much more easily in hot water than in cold water.
Acetanilide is converted in the human body into a toxic phenolic metabolite with analgesic effects.
Acetanilide is an example of an amide. Amides are a sort of exceedingly weak base. Imides, on the other hand, are less basic and react with strong bases to form salts.