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.
Oxidation of alkanols into “symmetric” esters with the system Ce(SO4)2—LiBr
作者:G. I. Nikishin、L. L. Sokova、N. I. Kapustina
DOI:10.1007/s11172-010-0006-6
日期:2009.2
A method for the synthesis of “symmetric” esters based on the oxidation of primary straight-and iso-chain aliphatic alcohols C6 —C11 with the system Ce(SO4)2—LiBr in water has been suggested.
Bohnsack, Chemische Berichte, 1941, vol. 74, p. 1575
作者:Bohnsack
DOI:——
日期:——
van Romburgh, Recueil des Travaux Chimiques des Pays-Bas, 1886, vol. 5, p. 236
作者:van Romburgh
DOI:——
日期:——
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.