化工社化工社 化学情報印刷レポート · 研究参考用
Diallyl Disulfide → Allicin
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diallyl Disulfide | HCID 16590 | — |
| 反応物 | Potassium peroxymonosulphate | HCID 10313463 | — |
| 溶媒 | Water ethanol | HCID 19096565 | — |
| 生成物 | Allicin | HCID 65036 | — |
反応手順
10 ml of diallyl disulphide (DADS) were stirred into 100 ml ethanol/water (1:1). 20 grams of potassium peroxymonosulfate (Oxone®) was added slowly over 2 hours, and stirred at below 10° C. until no further reaction was observed. The resultant solution was then filtered, and then extracted with diethyl ether (2×50 ml). The diethyl ether layers were combined and washed with 10% brine solution 2×50 ml. The ether layer was dried with magnesium sulfate then reduced to under vacuum. Removal of the solvent produced a yellow oil of pure allicin better than 90% (expressed as a % of pure material). The pure allicin may then be treated as per Example 1 for conversion to ajoene.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08623923B2 |
| 出典データセット | uspto-grants-2014_01 |
| ORD ID | ord-f08523db7f32422489394b230990a836 |
| 出典メモ | uspto-grants-2014_01 |