Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sorbitol | HCID 5780 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | 2,3,4,6-Tetra-O-methyl-D-glucose | HCID 14104335 | — |
| Reactant | HCID 15689262 | HCID 15689262 | — |
| Product | Maltitol | HCID 493591 | — |
Reaction Steps
Sugar components: (a) Acid hydrolysis using 1N sulfuric acid, and subsequent paper and gas-liquid chromatographic analyses confirmed the presence of equimolar D-glucose and D-sorbitol fractions; (b) Complete methylation, hydrolysis and subsequent gas-liquid chromatographic analysis confirmed the presence of equimolar 2,3,4,6-tetra-O-methyl-D-glucose and 1,2,3,5,6-penta-O-methyl-D-sorbitol fractions; (c) The high specific rotation, [α]D20, of +106.5° and the infrared absorption neighboring 840 cm-1 suggest the presence of an α-linkage between the glucose and sorbitol moieties; (d) Paper, gas-liquid and high-pressure liquid chromatographic analyses on the anhydrous crystals of maltitol gave the same single spot or peak at the same position as in the analyses on a commercial authentic maltitol preparation (special grade reagent).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04789559 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-ebc850133e3146a5ac194f0dd44c1b88 |
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| Source note | uspto-grants-1988_12 |
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