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Acetamide (systematic name: ethanamide) is an organic compound with the formula CH 3 CONH 2. It is an amide derived from ammonia and acetic acid. It finds some use as a plasticizer and as an industrial solvent. [5] The related compound N,N-dimethylacetamide (DMA) is more widely used, but it is not
As a source of amidine, acetamidine hydrochloride is a precursor to the industrial and laboratory synthesis of many nitrogen compounds.It reacts with β-dicarbonyls to produce substituted pyrimidines, [5] with acetaldehydes to form substituted imidazoles, [6] and with imidates to form substituted triazines.
In the usual implementation, hydrogen peroxide is used together with acetamide. This mixture does not react with ammonia directly but does so in the presence of methyl ethyl ketone to give the oxaziridine. Balanced equations for the individual steps are as follows. Imine formation through condensation: Me(Et)C=O + NH 3 → Me(Et)C=NH + H 2 O
A. Acamprosate; Acaprazine; Aceglutamide; Aceperone; 4-Acetamido-TEMPO; Acetazolamide; Acetergamine; Acetoacetamide; Acetoxolutamide; Aceturic acid; N-Acetyl-L-tyrosine
Dimethylacetamide is commonly used as a solvent for fibers (e.g., polyacrylonitrile, spandex) or in the adhesive industry. [5] It is also employed in the production of pharmaceuticals and plasticizers as a reaction medium. A solution of lithium chloride in DMAc (LiCl/DMAc) can dissolve cellulose. Unlike many other cellulose solvents, LiCl/DMAc ...
Acetanilide can be produced by reacting acetic anhydride with aniline: [7]. C 6 H 5 NH 2 + (CH 3 CO) 2 O → C 6 H 5 NHCOCH 3 + CH 3 COOH. The preparation used to be a traditional experiment in introductory organic chemistry lab classes, [8] but it has now been widely replaced by the preparation of either paracetamol or aspirin, both of which teach the same practical techniques (especially ...
Acetamide; Dichloroacetamide; N-Chlorosuccinimide; ... Chloroacetamide has been used as an herbicide, [5] preservative. [6] and in the manufacturing of pharmaceuticals.
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