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HRID 1871581作成日:2026年10月26日

Maltulose → Mannitol

https://huagongshe.com/reaction/1871581

反応式

関与物質

役割名称HCID仕込み量
反応物MaltuloseHCID 87177—
反応物TrehaluloseHCID 162104—
反応物LeucroseHCID 165577—
反応物GlyTouCan:G36918VOHCID 439559—
反応物(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—
生成物MannitolHCID 6251—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06103894
出典データセットuspto-grants-2000_08
ORD IDord-eca8e0b754634ef9a4ca71da2acfb9b8
出典メモuspto-grants-2000_08