Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | o-Tolylhydrazinium(1+) chloride | HCID 71554 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | D-Glucosone | HCID 159630 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Water | HCID 962 | — |
| Product | Sophorose | HCID 92797 | — |
Reaction Steps
This oligosaccharide (5 μmol), sodium acetate (10 μmol) and o-tolylhydrazine hydrochloride (30 μmol) were dissolved in 0.15 mL water in a small vial (Pierce reacti-vial, 0.2 mL capacity, with Tuf-bond Teflon-silicone cap seals). The vial was sealed under argon and warmed on a heating block to 70° C. for 6 hours; the solution became yellow over time and gave a yellow crystalline precipitate, which increased upon cooling to room temperature overnight. The water-insoluble material was the cleavage product, glucose o-tolylosazone (D-arabino-hexos-2-ulose o-tolylosazone. The water soluble fraction contained 2-Oβ-D-glucopyranosyl-D-glucose o-tolylhydrazone, and small amounts of D-glucose and the starting oligosaccharide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403927 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-554c93084ebf4c47970d9ec2a6fdea72 |
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| Source note | uspto-grants-1995_04 |
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