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HRID 131081作成日:2026年10月27日

Water → 4-{2-[2-(2-Methoxyethoxy)ethoxy]ethyl}nitrobenzene

https://huagongshe.com/reaction/131081

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-NitrophenolHCID 980—
反応物Potassium CarbonateHCID 11430—
反応物2-(2-(2-Methoxyethoxy)ethoxy)ethyl 4-methylbenzenesulfonateHCID 9948898—
溶媒DimethylformamideHCID 6228—
生成物4-{2-[2-(2-Methoxyethoxy)ethoxy]ethyl}nitrobenzeneHCID 6692772777.1%

反応条件

温度80 °C

反応手順

A portion of 13 (9.0 g, 28.3 mmol) was dissolved in 50 mL of dimethylformamide. Potassium carbonate (11.75 g, 85.0 mmol) and 4-nitrophenol (3.82 g, 27.5 mmol) were added. The solution was stirred at 80° C. for 16 hours. After cooling to room temperature, the solution was poured into water and extracted three times with methylene chloride. The combined organic layers were washed with water, then brine, dried over magnesium sulfate, filtered, and the solvent was removed by distillation at reduced pressure. Chromatography (silica, hexane:ethyl acetate, 1:2) was employed to isolate the product (5.71 g, 73% yield). IR (neat) 3109.2, 3078.2, 2878.5, 1726.3, 1588.1, 1511.2, 1337.1, 1106.7, 1050.3, 932.6, 845.5, 753.3, 656.1 cm−1. 1H NMR (CDCl3) δ 8.07 (d, J=9.3 Hz, 2H), 6.88 (d, J=9.3 Hz, 2H), 4.12 (app t, 2H), 3.79 (app t, 2H), 3.62 (m, 2H), 3.58 to 3.53 (m, 4H), 3.44 to 3.42 (m, 2 H), 3.26 (s, 3 H); 13C NMR (100 MHz, CDCl3) δ 164.29, 141.93, 126.24, 114.99, 72.29, 71.29, 71.03, 70.98, 69.77, 68.60, 59.44.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384815B2
出典データセットuspto-grants-2008_06
ORD IDord-5e97ae47f478442a93f38cf080cab1a8
出典メモuspto-grants-2008_06