Selective syntheses of aliphatic carboxylic acids, esters, and amides using sodium tetracarbonylferrate(-II) was written by Collman, James P.;Winter, Stanley R.;Komoto, Robert G.. And the article was included in Journal of the American Chemical Society in 1973.Application In Synthesis of Ethyl methyl adipate The following contents are mentioned in the article:
New routes have been developed for the conversion of alkyl halides and tosylates into carboxylic acids, esters, and amides using sodium tetracarbonylferrate(-II). Carboxylic acids are obtained from alkyl or acyl tetracarbonylferrate(0) intermediates using O2, NaClO, or I2/H2O. Esters and amides are obtained from the same intermediates using I2/ROH and I2/RR’NH resp. Advantages of these syntheses lie in their selectivity between halides and in their toleration of a wide range of functional groups including carbonyl groups. In addition, it is likely that the stereospecificity observed in one of our earlier ketone synthesis will be also found in these reactions. This study involved multiple reactions and reactants, such as Ethyl methyl adipate (cas: 18891-13-9Application In Synthesis of Ethyl methyl adipate).
Ethyl methyl adipate (cas: 18891-13-9) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. 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 Ethyl methyl adipate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics