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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23710생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물HexaneHCID 8058—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물Benzaldehyde, 4-(2-hydroxyethoxy)-HCID 89178—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehydeHCID 5795610149.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852731B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-80c3f0ea60a240ea855be153730b5b6d
출처 메모uspto-grants-2005_02