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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1871581Erstellt: 27. Oktober 2026

Maltulose → Mannitol

https://huagongshe.com/reaction/1871581

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMaltuloseHCID 87177—
EduktTrehaluloseHCID 162104—
EduktLeucroseHCID 165577—
EduktGlyTouCan:G36918VOHCID 439559—
Edukt(2S,3R,4S,5R,6R)-2-[(2R,3S,4S,5R)-4,5-dihydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol;hydrateHCID 66964417—
ProduktMannitolHCID 6251—

Reaktionsschritte

In another preferred embodiment, isomaltulose is hydrogenated. The composition of the reaction product here has a different composition than is expected from a conventional process, where about 50 wt.-% 1,1-GPM and 50 wt.-% 1,6-GPS are generated. The reaction product has a larger 1,1-GPM fraction and a smaller 1,6-GPS fraction. Advantageously, the process of the invention can also be used for hydrogenating trehalulose to 1,1-GPM and 1-0-α-D-glocupyranosil-D-sorbite (1,1-GPS), lactulose to lactite and 3-0-β-D-glucopyranosil-D-mannite, maltulose to 3-0-α-D-glucopyranosil-D-mannite and 4-0-α-D-glucopyranosil-D-sorbite (maltite), and leucrose to 5-0-α-D-glucopyranosil-D-sorbite (1,5-GPS) and 2-0-α-D-glocupyranosil-D-mannite (1,2-GPM). Advantageously, the product has a relatively higher 1,1-GPM fraction in the case of trehalulose, a relatively higher 3-0-α-D-glucopyranosil-D-mannite fraction in the case of maltulose, and a relatively higher 3-0-β-D-glucopyranosil-D-mannite fraction in the case of lactulose. When the aforedescribed glucopyranosil-substituted ketoses are hydrogenated, the invention thus produces an larger mannite epimer fraction and a smaller sorbite epimer fraction in the product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06103894
Quelldatensatzuspto-grants-2000_08
ORD IDord-eca8e0b754634ef9a4ca71da2acfb9b8
Quellennotizuspto-grants-2000_08