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HRID 1098622作成日:2026年10月27日

Phenol → 1-(2-Methoxy-ethoxy)-3-methyl-2-nitrobenzene

https://huagongshe.com/reaction/1098622

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物Potassium CarbonateHCID 11430—
反応物3-Methyl-2-nitrophenolHCID 21026—
反応物2-Bromoethyl methyl etherHCID 80972—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-(2-Methoxy-ethoxy)-3-methyl-2-nitrobenzeneHCID 12855496—

反応条件

温度50 °C

反応手順

The required 1-(2-methoxy-ethoxy)-3-methyl-2-nitrobenzene was prepared from 3-methyl-2-nitrophenol. To a stirred solution of the phenol (2.0 g, 13.1 mmol) in DMF (65 mL) was added potassium carbonate (2.16 g, 15.7 mmol) and bromoethyl methyl ether (1.47 mL, 15.7 mmol) at room temperature. After the mixture was stirred at 50° C. for 48 h, water was added. The mixture was extracted with EtOAc (3×), washed with brine, dried over anhydrous MgSO4 filtered and evaporated. After chromatographic purification on silica gel, 1-(2-methoxy-ethoxy)-3-methyl-2-nitrobenzene was obtained in 85% yield (2.34 g). 1H NMR (500 MHz, CDCl3) δ 7.28 (1H, t, J=8.0 Hz), 6.89 (1H, d, J=9.0 Hz), 6.85 (1H, d, J=8.0 Hz), 4.19 (2H, t, J=4.5 Hz), 3.72 (2H, t, J=5.0 Hz), 3.41 (3H, s), 2.30 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08143300B2
出典データセットuspto-grants-2012_03
ORD IDord-fdcb500e371e41eea1b41b94dc63b6b8
出典メモuspto-grants-2012_03