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HRID 23710作成日:2026年10月24日

Imidazole → 4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehyde

https://huagongshe.com/ja/reaction/23710

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物HexaneHCID 8058—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Benzaldehyde, 4-(2-hydroxyethoxy)-HCID 89178—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehydeHCID 5795610149.9%

反応手順

To 4-(2-hydroxyethoxy)benzaldehyde (commercial, 0.5 g, 3 mmol) dissolved in DMF (10 mL) is added imidazole (0.4 g, 6 mmol) and tert-butyldimethylsilylchloride (0.53 g, 3.5 mmol). Reaction mixture is stirred for 20 h. at room temperature. TLC analysis (hexane:ethyl acetate,7:3) shows small amounts of unreacted starting material. Additional tert-butyldimethylsilylchloride (0.25 g, 1 mmol) is added and stirring continued for 16 h. The reaction is quenched with saturated aqueous ammonium chloride (20 mL) and diluted further with ethyl ether (20 mL). Aqueous layer is separated and extracted thrice with ether (10 mL). Combined organics dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue is purified by flash chromatography on silica gel using a gradient of 2% to 5% ethyl acetate in hexanes to provide 0.42 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852731B2
出典データセットuspto-grants-2005_02
ORD IDord-80c3f0ea60a240ea855be153730b5b6d
出典メモuspto-grants-2005_02