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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468086Generated: October 25, 2026

Diallyl Disulfide → Allicin

https://huagongshe.com/reaction/468086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiallyl DisulfideHCID 16590—
ReactantPotassium peroxymonosulphateHCID 10313463—
SolventWater ethanolHCID 19096565—
ProductAllicinHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623923B2
Source datasetuspto-grants-2014_01
ORD IDord-f08523db7f32422489394b230990a836
Source noteuspto-grants-2014_01