HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycerol → (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycerol | HCID 753 | — |
| Reactant | Erythritol | HCID 222285 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
Reaction Steps
Separately, the polyol-type ganoderan was kept at 90°-100° C. for 1-2 hours in 0.05-0.1M sulfuric acid to obtain, as well as glycerol and erythritol, an insoluble substance. Hydrolysis of the insoluble substance gave D-glucose as sole product, while hydrolysis of a methylated polyol-type ganoderan gave a substantial amount of 2,4,6-tri-O-methyl-D-glucose. By exposure to the action of exo-beta-1,3 glucanase, only D-glucose was obtained. These facts confirm that the backbone of ganoderan consists of beta-1,3-linked D-glucopyranose residues.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04769363 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-79b1917a9c6a4120a5e74642eee839ec |
| Source note | uspto-grants-1988_09 |