HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium Hydroxide → HCID 54187119, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | alpha-D-Glucopyranosyl bromide, tetraacetate | HCID 101776 | — |
| Edukt | Pachypodol | HCID 5281677 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | HCID 54187119 | HCID 54187119 | 106,1% |
Reaktionsschritte
To an ice-cooled solution containing 250 mg of 4',5-dihydroxy-3,3',7-trimethoxyflavone in 10 ml of acetone were alternately added a solution of 400 mg of 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide in 10 ml of acetone, and 5 ml of 0.8% aqueous sodium hydroxide over 30 minutes, while stirring. After allowing the reaction mixture to stand at room temperature for 3 hours, 20 ml of 0.2% aqueous sodium hydroxide were added thereto. Stirring was continued at room temperature for 3 hours, during which time crystallization took place. The crystals were collected by filtration and recrystallized from ethanol to give 390 mg (80% yield) of 4'-(β-D-glucopyranosyloxy)-5-hydroxy-3,3',7-trimethoxyflavone as pale yellow needles: m.p. 203°-204° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04352792 |
| Quelldatensatz | uspto-grants-1982_10 |
| ORD ID | ord-49a6629c73304c02a55efa2c0ae4ea4d |
| Quellennotiz | uspto-grants-1982_10 |