Primary alkanols: oxidative homocondensation in water and cross-condensation in methanol
作者:G. I. Nikishin、L. L. Sokova、A. O. Terent´ev、N. I. Kapustina
DOI:10.1007/s11172-015-1236-4
日期:2015.12
Water was used as a reaction medium and a reagent in oxidation of primary alkanols to dimeric esters and alkanoic acids using either molecular bromine or a hydrogen peroxide—hydrobromic acid mixture as the oxidants. The similar reaction in methanol produced methyl alkanoates.
Selective oxidation of primary alkanols into the “symmetrical” esters with the H2O2-MBr-HCl system
作者:G. I. Nikishin、L. L. Sokova、N. I. Kapustina
DOI:10.1007/s11172-011-0050-x
日期:2011.2
Oxidation of linear or branched primary alkanols with H2O2-MBr (M = Li, Na, K)-HCl system in water affords the corresponding “symmetrical” esters in almost quantitative yield.