HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → alpha-D-Glucopyranosyl pentaacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Alpha-D-Glucose | HCID 79025 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | alpha-D-Glucopyranosyl pentaacetate | HCID 2723636 | 88% |
Reaction Steps
Analogously, as described in the synthesis of title compound Aa), the reaction of 100 g (555.0 mmol) of α-D-glucopyranose with a mixture of 1000 ml of absolute pyridine and 1000 ml of acetic acid anhydride after working-up and recrystallization from 95% aqueous ethanol yields 190.6 g (88.0%) of the above-mentioned title compound as a colorless and crystalline compound. By 1H-NMR-spectroscopic study of the title compound that is thus obtained, it was possible to determine the α to β-ratio of two possible anomers with ≧98:2. Accordingly, the title compound is the exclusively α-configured anomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06447749B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-452fc11b03e643f3b000291e3c842f68 |
| Source note | uspto-grants-2002_09 |