Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Kasugamycin hydrochloride | HCID 88045 | — |
| Solvent | Water | HCID 962 | — |
| Product | An inositol | HCID 892 | 15% |
Reaction Steps
Kasugamycin hydrochloride (1 g), 5 mL deionized H2O and Diaion™ SK 116 resin (6 g) were combined and heated 4 h at 85° C., and then at 100° C. for 3 h. The catalyst was removed by filtration through a course scintered glass funnel and washed with deionized H2O (20 mL). The mixture was purified as above, using ion exchange resins and charcoal, yielding D-chiro-inositol (15%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06342645B2 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-ac45ec86dee24ca68aa5c8edcf26b7ba |
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| Source note | uspto-grants-2002_01 |
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