Regioselective Synthesis of N2-Aryl 1,2,3-Triazoles via Electro-oxidative Coupling of Enamines and Aryldiazonium Salts was written by Baidya, Mrinmay;Mallick, Samrat;De Sarkar, Suman. And the article was included in Organic Letters in 2022.Quality Control of Ethyl 3-oxo-3-(m-tolyl)propanoate This article mentions the following:
An efficient synthetic route for the construction of N2-aryl 1,2,3-triazoles I (R = Me, cyclopropyl, 4-chlorophenyl, thiophen-2-yl, etc.; R1 = COOMe, COOEt, C(O)Me; Ar = Ph, 3-chlorophenyl, 2,4,6-trimethylphenyl, etc.) is reported via sequential C-N bond formation and electro-oxidative N-N coupling under metal-free conditions. Readily accessible 2-aminoacrylates NH2RC=CHCOOR1 and aryldiazonium salts ArN2+BF4– were used as starting materials, and the developed protocol displays excellent functional group tolerance, allowing an extensive range of substrate scope up to 91% isolated yield. Various mechanistic studies, along with the isolation of an intermediate adduct, refer to successive ionic and radical reaction sequences. In the experiment, the researchers used many compounds, for example, Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9Quality Control of Ethyl 3-oxo-3-(m-tolyl)propanoate).
Ethyl 3-oxo-3-(m-tolyl)propanoate (cas: 33166-79-9) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Quality Control of Ethyl 3-oxo-3-(m-tolyl)propanoate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics