反応式
[CH2:1]([S:4][S:5][CH2:6][CH:7]=[CH2:8])[CH:2]=[CH2:3].S([O-])(O[O-])(=O)=[O:10].[K+].[K+]>C(O)C.O>[CH2:3]=[CH:2][CH2:1][S:4](=[O:10])[S:5][CH2:6][CH:7]=[CH2:8]参加物
4
実験手順
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.
後処理
- filtrationThe resultant solution was then filtered
- extractionextracted with diethyl ether (2×50 ml)
- washwashed with 10% brine solution 2×50 ml
- dry with materialThe ether layer was dried with magnesium sulfate
- customRemoval of the solvent
出典と根拠
- ORDレコード
- ord-f08523db7f32422489394b230990a836
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08623923B2
関連ノート
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