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Sodium Hydroxide → 5-hydroxy-3,7,3'-trimethoxyflavone-4'-O-beta-D-glucoside
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | alpha-D-Glucopyranosyl bromide, tetraacetate | HCID 101776 | — |
| 反応物 | Pachypodol | HCID 5281677 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 5-hydroxy-3,7,3'-trimethoxyflavone-4'-O-beta-D-glucoside | HCID 54187119 | 106.1% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04352792 |
| 出典データセット | uspto-grants-1982_10 |
| ORD ID | ord-49a6629c73304c02a55efa2c0ae4ea4d |
| 出典メモ | uspto-grants-1982_10 |