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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1098622Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1098622

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktPotassium CarbonateHCID 11430—
Edukt3-Methyl-2-nitrophenolHCID 21026—
Edukt2-Bromoethyl methyl etherHCID 80972—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(2-Methoxy-ethoxy)-3-methyl-2-nitrobenzeneHCID 12855496—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08143300B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-fdcb500e371e41eea1b41b94dc63b6b8
Quellennotizuspto-grants-2012_03