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HRID 11506作成日:2026年10月27日

p-Fluoronitrobenzene → N,N-diethyl-3-(4-nitrophenoxy)propan-1-amine

https://huagongshe.com/reaction/11506

反応式

関与物質

役割名称HCID仕込み量
反応物p-FluoronitrobenzeneHCID 9590—
反応物3-(Diethylamino)-1-propanolHCID 12159—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物N,N-diethyl-3-(4-nitrophenoxy)propan-1-amineHCID 205788671.2%

反応条件

温度0 °C

反応手順

A solution of 3-diethylamino-1-propanol (2.97 mL, 20 mmol) in THF (40 mL) at 0° C. is treated potassium tert-butoxide (2.36 g, 1.05 equiv.) in one portion. The reaction mixture is stirred at 0° C. for 5 min during which time it becomes reddish brown. Neat 1-fluoro-4-nitrobenzene (2.82 g, 1 equiv.) is added dropwise and the ice-bath is removed. The reaction mixture is stirred at room temperature for 15 min. The dark green reaction mixture is quenched with ice-water (300 mL), and extracted with EtOAc (2×200 mL). The combined organic extracts are washed with water (2×300 mL) and brine (1×300 mL) and dried over anhydrous Na2SO4. The oily brown residue obtained after evaporation, is purified by chromatography, (silica gel, 1:4 MeOH:CHCl3) to give the named compound as a brown oil (3.59 g, 71%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098236B2
出典データセットuspto-grants-2006_08
ORD IDord-b8a7013060c64ea0a72ae1347253d224
出典メモuspto-grants-2006_08