In 2019,Chemical Communications (Cambridge, United Kingdom) included an article by Shen, Ni; Cheung, Chi Wai; Ma, Jun-An. Name: 3-Chloro-4-fluoronitrobenzene. The article was titled 《Direct amide synthesis via Ni-mediated aminocarbonylation of arylboronic acids with CO and nitroarenes》. The information in the text is summarized as follows:
An alternative and unconventional approach of an aminocarbonylation reaction to access aryl amides from readily available and low-cost arylboronic acids and nitroarenes was described. Nickel metal served as both reductant and catalyst in this direct aminocarbonylation. This protocol exhibited a good functional group compatibility and allows a variety of aryl amides to be synthesized, including several drug-like mols. In the part of experimental materials, we found many familiar compounds, such as 3-Chloro-4-fluoronitrobenzene(cas: 350-30-1Name: 3-Chloro-4-fluoronitrobenzene)
3-Chloro-4-fluoronitrobenzene(cas: 350-30-1) belongs to organochlorine compounds. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. Name: 3-Chloro-4-fluoronitrobenzene The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics