反応式
[CH:1]1[C:6](=[O:7])[C:5]([OH:8])=[CH:4][O:3][C:2]=1[CH2:9]O.S(Cl)([Cl:13])=O>CN(C)C=O>[CH:1]1[C:6](=[O:7])[C:5]([OH:8])=[CH:4][O:3][C:2]=1[CH2:9][Cl:13]参加物
4
反応条件
- 温度
- 10 °C
実験手順
50 g(351.8 mmol) of kojic acid was dissolved in 250 ml of N,N-dimethylformamide. The resulting solution was cooled in a ice bath of 10° C. and 30 ml(411.3 mmole) of thionyl chloride was added dropwise thereto. The mixture was stirred at a room temperature for 2 hours and 2000 ml of ice water was added. The precipitates were filtered and dissolved into 1000 ml of ethyl acetate. The reaction product was dried over magnesium sulfate, decolored with active charcoal and filtered. The filtrate was concentrated and hexane was added to give crystals, which was then dried under vacuum to give 37.5 g(66.83%) of the desired chlorokojic acid as a yellow solid.
後処理
- filtrationThe precipitates were filtered
- dissolutiondissolved into 1000 ml of ethyl acetate
- dry with materialThe reaction product was dried over magnesium sulfate
- filtrationfiltered
- concentrationThe filtrate was concentrated
- additionhexane was added
- customto give crystals, which
- customwas then dried under vacuum
出典と根拠
- ORDレコード
- ord-8e4894ec7a404f27b9bad3889dbbf050
- 出典データセット
- uspto-grants-1996_06
- 特許番号
- US05523421
関連ノート
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