The author of 《New Synthesis of 2-Oxoalkanamide Oximes》 were Mantrov, S. N.; Lapina, Yu. M.; Shukhtina, E. A.. And the article was published in Russian Journal of Organic Chemistry in 2019. Name: 3,5-Dibromoaniline The author mentioned the following in the article:
Reactions of α-halocarboxylic acid amides R1NHC(O)CH(X)R (R = H, Me, Bu; R1 = C6H5, 4-BrC6H4, 1,3-thiazol-2-yl, etc.; X = Cl, Br) with 3 equiv of hydroxylamine hydrochloride in the presence of bases involves formation of products of nucleophilic substitution of the halogen atom and their subsequent oxidation to the corresponding oximes R1NHC(O)C(=NOH)R. This one-pot transformation can be accomplished in various aprotic solvents or ethanol at 80°C. DMSO as solvent ensures the highest selectivity for the oxidation products. The yields of N-substituted 2-(hydroxyimino)carboxylic acid amides range from 22 to 92%. The results came from multiple reactions, including the reaction of 3,5-Dibromoaniline(cas: 626-40-4Name: 3,5-Dibromoaniline)
3,5-Dibromoaniline(cas: 626-40-4) belongs to anime. The methylamines occur in small amounts in some plants. Many polyfunctional amines (i.e., those having other functional groups in the molecule) occur as alkaloids in plants—for example, mescaline, 2-(3,4,5-trimethoxyphenyl)ethylamine; the cyclic amines nicotine, atropine, morphine, and cocaine; and the quaternary salt choline, N-(2-hydroxyethyl)trimethylammonium chloride, which is present in nerve synapses and in plant and animal cells.Name: 3,5-Dibromoaniline
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary