Electrochemical esterification via oxidative coupling of aldehydes and alcohols was written by Smeyne, Dylan;Verboom, Katherine;Bryan, Maria;LoBue, James;Shaikh, Abid. And the article was included in Tetrahedron Letters in 2021.Application In Synthesis of Methyl heptanoate The following contents are mentioned in the article:
An electrolytic method for the direct oxidative coupling of aldehydes with alcs. to produce esters is described. This method involves anodic oxidation in presence of TBAF as supporting electrolyte in an undivided electrochem. cell equipped with graphite electrodes. This method successfully couples a wide range of alcs. to benzaldehydes with yields ranging from 70 to 90%. The protocol is easy to perform at a constant voltage conditions and offers a sustainable alternative over conventional methods. This study involved multiple reactions and reactants, such as Methyl heptanoate (cas: 106-73-0Application In Synthesis of Methyl heptanoate).
Methyl heptanoate (cas: 106-73-0) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Application In Synthesis of Methyl heptanoate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics