Reaktionsgleichung
[CH3:1][C:2]1[C:3](=[O:10])[C:4]([CH3:9])=[CH:5][C:6](=[O:8])[CH:7]=1.Cl.[C:12]([O:15][CH2:16][CH3:17])(=[O:14])[CH3:13]>C1COCC1>[OH:8][C:6]1([CH2:13][C:12]([O:15][CH2:16][CH3:17])=[O:14])[CH:7]=[C:2]([CH3:1])[C:3](=[O:10])[C:4]([CH3:9])=[CH:5]1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Under argon atmosphere, a solution of 0.45 g (3.33 mmol) of 2,6-dimethyl-p-benzoquinone in 3 mL of THF was added dropwise while stirring at 0˜5° C. The mixture was stirred at 20˜25° C. for 1 hour. 5 mL of 1N hydrochloric acid was added dropwise at 20° C. or lower, followed by dilution with 25 mL of ethyl acetate. Then, the layers were separated. The organic layer was washed successively with 5 mL (×2) of 1N hydrochloric acid, 5 mL of water, 10 mL (×2) of an aqueous saturated sodium bicarbonate solution, and 5 mL (×2) of an aqueous saturated sodium chloride solution. After washing, the organic layer was dried with anhydrous magnesium sulfate. After concentration under reduced pressure, purification with silica gel column (developing solvent; ethyl acetate/n-hexane=1/3) afforded 0.60 g of the desired product (yield 80%).
Aufarbeitung
- stirringThe mixture was stirred at 20˜25° C. for 1 hour
- customThen, the layers were separated
- washThe organic layer was washed successively with 5 mL (×2) of 1N hydrochloric acid, 5 mL of water, 10 mL (×2) of an aqueous saturated sodium bicarbonate solution, and 5 mL (×2) of an aqueous saturated sodium chloride solution
- washAfter washing
- dry with materialthe organic layer was dried with anhydrous magnesium sulfate
- concentrationAfter concentration
- customunder reduced pressure, purification with silica gel column (developing solvent; ethyl acetate/n-hexane=1/3)
Quellen und Nachweise
- ORD-Eintrag
- ord-a93bed300ed24f88a15c9b0880ac34ce
- Quelldatensatz
- uspto-grants-2010_02
- Patentnummer
- US07662974B2
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