HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250811Generated: November 1, 2026
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal → HCID 178418489, compound
https://huagongshe.com/reaction/1250811
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178418489 | HCID 178418489 | — |
Reaction Steps
As illustrated in FIG. 2, addition of glucose and ethanol resulted in the production of an significantly increased amount of xylitol, so that a considerable effect of their addition was observed. In the case where no carbon source was added, D-arabitol was oxidized substantially completely to D-xylulose. Even in the reaction without addition of any carbon source, prevention of pH at the time of reaction from decreasing by addition of calcium carbonate resulted in a slight increase in the yield of xylitol, more particularly 1.23% (w/v) xylitol was produced in 24 hours' reaction. However, a portion of D-xylulose remained unreacted, no further increase in yield did occur. In contrast, with addition of a carbon source, D-xylulose was reduced to xylitol substantially completely, and at the point in time of 24 hours, xylitol was produced and accumulated in a yield as high as 5.24% (w/v) (98% based on D-arabitol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06340582B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-41441c6243624174b411c2a96037bb66 |
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| Source note | uspto-grants-2002_01 |
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