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HRID 7237作成日:2026年10月27日

tert-Butyldimethyl(4-nitrophenoxy)silane → 4-((Tert-butyldimethylsilyl)oxy)aniline

https://huagongshe.com/reaction/7237

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyldimethyl(4-nitrophenoxy)silaneHCID 532659—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物4-((Tert-butyldimethylsilyl)oxy)anilineHCID 11715553—

反応手順

A solution of 1-nitro4-(1,1,2,2-tetramethyl-1-silapropoxy)benzene (7.8 g, 30.8 mmol) (from Example 19a supra) and 10% Pd/C (0.70 g) (Aldrich) in ethyl acetate (100 mL) was hydrogenated for 1 day. The reaction mixture was filtered though Celite® and concentrated. The residue was purified by flash chromatography eluting with ethyl acetate/hexanes (1:9 V/N)) to afford 4-(1,1,2,2-tetramethyl-1-silapropoxy)phenylamine. (Yield 6.7 g, 97%).

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-a803ccb62a404612ad797f6d240d47bb
出典メモuspto-grants-2006_08