Methane → Isomaltitol
Reaktionsgleichung
[CH2:1]([OH:23])[C@H:2]1[O:7][C@H:6]([O:8][CH2:9][C@H:10]2[O:15][CH:14]([OH:16])[C@H:13]([OH:17])[C@@H:12]([OH:18])[C@@H:11]2[OH:19])[C@H:5]([OH:20])[C@@H:4]([OH:21])[C@@H:3]1[OH:22].C>>[CH2:1]([OH:23])[C@H:2]1[O:7][C@H:6]([O:8][CH2:9][C@@H:10]([OH:15])[C@@H:11]([OH:19])[C@H:12]([OH:18])[C@@H:13]([OH:17])[CH2:14][OH:16])[C@H:5]([OH:20])[C@@H:4]([OH:21])[C@@H:3]1[OH:22]Komponenten
3
Versuchsvorschrift
An isomaltose content syrup, obtained by the method in Example A-1, was hydrogenated in accordance with the method in Experiment 36, and the resulting mixture was in a usual manner decolored with an activated charcoal, desalted for purification with ion-exchange resins in H- and OH-forms, and concentrated to give a concentration of about 73%. The concentrate was spray dried in a usual manner to obtain a high isomaltitol content powder, containing 43.3% of isomaltitol, 37.8% of ring-opened tetrasaccharide, 13.8% of cyclotetrasaccharide, and 3.5% of other sugar alcohols, in a yield of about 80%.
Aufarbeitung
- customdesalted for purification with ion-exchange resins in H-
- concentrationOH-forms, and concentrated