化工社化工社 化学情報印刷レポート · 研究参考用
Hydrogen Peroxide → 3,4,6-Trihydroxy-8-((2R,3R)-3,5,7-trihydroxychroman-2-yl)-1-((2R,3S)-3,5,7-trihydroxychroman-2-yl)-5H-benzo[7]annulen-5-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Peroxide | HCID 784 | — |
| 反応物 | 2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol | HCID 1203 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 3,4,6-Trihydroxy-8-((2R,3R)-3,5,7-trihydroxychroman-2-yl)-1-((2R,3S)-3,5,7-trihydroxychroman-2-yl)-5H-benzo[7]annulen-5-one | HCID 44610426 | — |
反応手順
C (catechin) (0.8 g) and EGC (0.8 g) were dissolved in a mixture of acetone-pH 5.0 phosphate citrate buffer (1:10, v/v, 50 mL), which contained 4 mg horseradish peroxidase. While being stirred, 2.0 mL of 3.13% H2O2 was added four times during 45 minutes. The reaction mixture was extracted by ethyl acetate (50 mL×3). After concentration, the residue was subjected to Sephadex LH 20 column eluted with acetone-water solvent system (45%). 120 mg neotheaflavin was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07087790B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-aaaa2f5ab5bb40d1ae85edc2fc0aab4a |
| 出典メモ | uspto-grants-2006_08 |