Wi, Eun Hye’s team published research in Inorganic Chemistry in 2019 | CAS: 4755-77-5

Ethyl oxalyl monochloride(cas: 4755-77-5) belongs to acyl chlorides. In the laboratory, acyl chlorides are generally prepared by treating carboxylic acids with thionyl chloride (SOCl2). The reaction is catalyzed by dimethylformamide and other additives.Application In Synthesis of Ethyl oxalyl monochloride

In 2019,Inorganic Chemistry included an article by Wi, Eun Hye; Ryu, Ji Yeon; Lee, Seul Gi; Farwa, Ume; Pait, Moumita; Lee, Sunwoo; Cho, Sung; Lee, Junseong. Application In Synthesis of Ethyl oxalyl monochloride. The article was titled 《Selective Self-Assembly of a Rectangular Ruthenium Supramolecule from an Unsymmetrical Bridging Unit》. The information in the text is summarized as follows:

Herein, the authors report the synthesis of an unsym. diruthenium bridging unit containing a multidentate oxamate ligand and the subsequent formation of a rectangular supramol. The reaction of oxamate 1, 2-((4-bromo-2,6-dimethylphenyl)amino)-2-oxo-HOAc, and [(p-cymene)RuCl2]2 affords a novel unsym. diruthenium acceptor clip 2, where two Ru metal centers are ligated with either [O,O] or [N,O]. The mol. clip 2 and bipyridine donor self-assemble to form two-dimensional rectangular supramol. 3. Self-assembly can produce seven possible isomers depending on the position of the substituted bromoaryl groups. However, 1H NMR spectroscopic study indicated only two different isomers in the reaction mixture A single isomer is isolated via crystallization, and x-ray crystallog. confirms that the product is a C1 sym. two-dimensional rectangular supramol., in which two bromoaryl groups are located in the farthest position from each other. Theor. calculations suggest that the self-assembly of supramol. 3 occurred via 1:1 adducts of the diruthenium mol. clip and bipyridine as an intermediate to predominantly form a single isomer. In addition to this study using Ethyl oxalyl monochloride, there are many other studies that have used Ethyl oxalyl monochloride(cas: 4755-77-5Application In Synthesis of Ethyl oxalyl monochloride) was used in this study.

Ethyl oxalyl monochloride(cas: 4755-77-5) belongs to acyl chlorides. In the laboratory, acyl chlorides are generally prepared by treating carboxylic acids with thionyl chloride (SOCl2). The reaction is catalyzed by dimethylformamide and other additives.Application In Synthesis of Ethyl oxalyl monochloride

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