Formula: C3H3ClO3In 2022 ,《Silver-catalysed double decarboxylative addition-cyclization-elimination cascade sequence for the synthesis of quinolin-2-ones》 appeared in Organic & Biomolecular Chemistry. The author of the article were Mazodze, C. Munashe; Petersen, Wade F.. The article conveys some information:
An atom-efficient silver-catalyzed double carboxylative strategy for the one-step synthesis of quinolin-2-ones I [R1 = H, Me, CF3; R2 = H, Me; R1R2 = CH2CH2CH2, CH2(CH2)2CH2; R3 = Me, Bn, Ph, etc.; R4 = H, 6-F, 6-OMe, etc.] via an addition-cyclization-elimination cascade sequence of oxamic acids to acrylic acids, mediated either thermally or photochem., was reported. The reaction was applicable to the synthesis of a broad range of quinolin-2-ones and featured a double-disconnection approach that constructed the quinolin-2-one core via the formal and direct addition of a C(sp2)-H/C(sp2)-H olefin moiety to a phenylformamide precursor. The experimental process involved the reaction of Methyl 2-chloro-2-oxoacetate(cas: 5781-53-3Formula: C3H3ClO3)
Methyl 2-chloro-2-oxoacetate(cas: 5781-53-3) belongs to acyl chlorides. Lacking the ability to form hydrogen bonds, acyl chlorides have lower boiling and melting points than similar carboxylic acids. For example, acetic acid boils at 118 °C, whereas acetyl chloride boils at 51 °C. Like most carbonyl compounds, infrared spectroscopy reveals a band near 1750 cm−1.Formula: C3H3ClO3
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics