Methane → Isomaltitol

HRID 734173

Reaktionsgleichung

Reaktionsgleichung von HRID 734173
[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

Edukt 2

HCID 297MethaneHCID 439193Isomaltose

Produkt 1

HCID 94169IsomaltitolAusbeute 80 %

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

  1. customdesalted for purification with ion-exchange resins in H-
  2. concentrationOH-forms, and concentrated
  3. customto give a concentration of about 73%
  4. customdried in a usual manner

Quellen und Nachweise

ORD-Eintrag
ord-a50546cf46fe49f89113277a29d65e4f
Quelldatensatz
uspto-grants-2009_09
Patentnummer
US07592160B2

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