Alkaline degradation of monosaccharides III. Influence of reaction parameters upon the final product composition
- 1 January 1986
- journal article
- research article
- Published by Wiley in Recueil des Travaux Chimiques des Pays-Bas
- Vol. 105 (6) , 176-183
- https://doi.org/10.1002/recl.19861050603
Abstract
A systematic investigation of the alkaline degradation of monosaccharides is presented. The influence of several parameters upon the degradation reaction has been determined by analysis of the reaction products using HPLC and, in some cases, GC. The HO− and the monosaccharide concentrations markedly influence the final product composition with respect to both the amount of C1 to C6 acids and the formation of oligomeric acidic products, the so‐called > C6 acids. Maximum yields of these > C6 acids, up to 50 mol‐C6‐%, are obtained at an HO− concentration of between 10−3 M and 10−2 M when the monosaccharide concentration exceeds 10−2 M. The presence of divalent calcium increases the retro‐aldolization of monosaccharides in alkaline medium, as illustrated by the enhanced production of lactic acid, by complexation with, for instance, d‐fructose. Borate partly protects monosaccharides against alkaline degradation through their borate esters, whilst the amount of saccharinic acids in the degradation product mixture is doubled. On the other hand, neither chloride and carbonate nor the reaction temperature influences the final product composition. Alkaline degradation experiments with pyruvaldehyde, glyceraldehyde and 1,3‐dihydroxyacetone, all assumed to be reaction intermediates, indicate that aldolization of (di)carbonyl compounds causes the formation of substantial amounts of > C6 acids.Funding Information
- CSM Suiker B.V
This publication has 20 references indexed in Scilit:
- Studies on borate esters III. Borate esters of D‐mannitol, D‐glucitol, D‐fructose and D‐glucose in waterRecueil des Travaux Chimiques des Pays-Bas, 1985
- Alkaline Degradation of Cellobiose, 3.6-Anhydro-4-O-(β-D-Gluc0pyranosyl)-D-Glucose, 3,6-Anhydr0-4-0-Methyl-D-Glucose, and D-Glucose1Journal of Wood Chemistry and Technology, 1982
- Enolisation and isomerisation of monosaccharides in aqueous, alkaline solutionCarbohydrate Research, 1979
- Ionization and mutarotation of hexoses in aqueous alkaline solution as studied by 13C NMR spectroscopyRecueil des Travaux Chimiques des Pays-Bas, 1979
- Alkali and Oxygen--Alkali Treatment of 4-Deoxy-2,3-hexodiulose and 3-Deoxy-erythro-pentose.Acta Chemica Scandinavica, 1977
- Degradation of Cellobiose in Hydroxide and Hydrogen Carbonate Solution.Acta Chemica Scandinavica, 1976
- Effect of Borate on the Alkali-catalyzed Isomerization of Sugars1Journal of the American Chemical Society, 1960
- The mutarotation and ionization of D-glucose in alkaline solution IIRecueil des Travaux Chimiques des Pays-Bas, 1957
- The mutarotation and ionization of d‐glucose in alkaline solutionRecueil des Travaux Chimiques des Pays-Bas, 1954
- Action des alcalis sur les sucres, II. Transformation réciproque des uns dans les autres des sucres glucose, fructose et mannoseRecueil des Travaux Chimiques des Pays-Bas, 1895