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HRID 1161508作成日:2026年10月27日

Imidazole → 3,4-Dimethoxy-5-triisopropylsilanyloxybenzaldehyde

https://huagongshe.com/reaction/1161508

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物WaterHCID 962—
反応物Triisopropylsilyl chlorideHCID 139400—
反応物3,4-Dimethoxy-5-hydroxybenzaldehydeHCID 141513—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物3,4-Dimethoxy-5-triisopropylsilanyloxybenzaldehydeHCID 86617921—

反応手順

To a solution of 3.2 g of 3-hydroxy-4,5-dimethoxybenzaldehyde in 50 ml of DMF there were added 1.49 g of imidazole and 4.5 ml of chlorotriisopropylsilane. The mixture was stirred at room temperature for 21 hours and 30 minutes. Water was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was washed with ice-cooled 1N hydrochloric acid, water, saturated aqueous sodium hydrogencarbonate, water and saturated brine in that order, and dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give 3,4-dimethoxy-5-triisopropylsilanyloxybenzaldehyde (6.08 g) as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07816522B2
出典データセットuspto-grants-2010_10
ORD IDord-ce3e7d53c13e4a0590460b96addc9d58
出典メモuspto-grants-2010_10