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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401611Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/401611

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
PatentnummerUS08741942B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-5b8c2a2be6f74fb8b7a7f609036c07b5
Quellennotizuspto-grants-2014_06