A facile, catalytic and environmentally benign method for esterification of carboxylic acids and transesterification of carboxylic esters with nearly equimolar amounts of alcohols was written by Bose, D. Subhas;Satyender, Apuri;Das, A. P. Rudra;Mereyala, Hari Babu. And the article was included in Synthesis in 2006.Application In Synthesis of Di-tert-butyl decanedioate The following contents are mentioned in the article:
A practical and green chem. process for the esterification of carboxylic acids with alcs. and transesterification of carboxylic esters in good to excellent yields by using K5CoW12O14·3H2O (0.1 mol%) as catalyst is reported. The catalyst exhibited remarkable reusable activity. This study involved multiple reactions and reactants, such as Di-tert-butyl decanedioate (cas: 143050-66-2Application In Synthesis of Di-tert-butyl decanedioate).
Di-tert-butyl decanedioate (cas: 143050-66-2) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. 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.Application In Synthesis of Di-tert-butyl decanedioate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics