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HRID 7236作成日:2026年10月24日

Imidazole → tert-Butyldimethyl(4-nitrophenoxy)silane

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

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物4-NitrophenolHCID 980—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyldimethyl(4-nitrophenoxy)silaneHCID 532659—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084270B2
出典データセットuspto-grants-2006_08
ORD IDord-fdb8a9152bfd4faca050f70d5c0c0d5b
出典メモuspto-grants-2006_08