HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diallyl Disulfide → Allicin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diallyl Disulfide | HCID 16590 | — |
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | Allicin | HCID 65036 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08623923B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-f08523db7f32422489394b230990a836 |
| Source note | uspto-grants-2014_01 |