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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7236생성일: 2026년 10월 23일

Imidazole → tert-Butyldimethyl(4-nitrophenoxy)silane

https://huagongshe.com/ko/reaction/7236

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물4-NitrophenolHCID 980—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
용매DimethylformamideHCID 6228—
생성물tert-Butyldimethyl(4-nitrophenoxy)silaneHCID 532659—

반응 단계

To a solution of 4-nitrophenol (5.0 g, 35.9 mmol) (Aldrich) in dimethylformamide (50 mL) was added imidazole (3.18 g, 46.7 mmol) (Aldrich) and t-butyldimethylsilyl chloride (6.49 g, 43.1 mmol) (Avocado Research Chemicals Ltd.). The reaction mixture was stirred at room temperature for 1 day. TLC analysis showed starting material was still present. Another portion of t-butyldimethylsilyl chloride (1.0 g, 6.63 mmol) was added and the mixture was stirred at room temperature for another 1 day. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (200 mL) and washed with a mixture of water (100 mL) and aqueous 1N HCl (80 mL). The organic layer was then washed with water, saturated aqueous sodium bicarbonate solution and brine, dried (MgSO4), filtered and concentrated. The residue was purified by flash chromatography eluting with ethyl acetate/hexanes (1:9, V/V) to afford 1-nitro-4-(1,1,2,2-tetramethyl-1-silapropoxy)benzene. (Yield 7.8 g, 86%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084270B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-fdb8a9152bfd4faca050f70d5c0c0d5b
출처 메모uspto-grants-2006_08