Imidazole → (2E)-3-[4-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-3,5-dimethoxyphenyl]-2-propenoic Acid

関与物質

反応手順

3,5-dimethoxy-4-hydroxy-cinnamic acid (3 g, 13.38 mmol) and imidazole (2.73 g, 40.14 mmol) were charged in a 500 mL round-bottom flask and dissolved in 15 mL of dimethylformamide. Tert-butyldimethylsilyl chloride (4.23 g, 28.09 mmol) was added thereto at 0° C., followed by stirring for 1 hour. The reaction liquid was concentrated by distillation under reduced pressure and dichloromethane (50 mL) was added thereto, followed by washing with water. The organic layer was dried over anhydrous magnesium sulfate, concentrated and dissolved in tetrahydrofuran (59 mL)/methanol (167 mL), and a 0.00035M potassium carbonate aqueous solution (62 mL) was added thereto, followed by stirring for 1 hour. After being concentrated by distillation under reduced pressure, the resulting solid was filtered, washed with water, and dried under vacuum to afford the title compound.

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