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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29231Erstellt: 24. Oktober 2026

Methanol → 4-Bromo-2-methoxybenzonitrile

https://huagongshe.com/de/reaction/29231

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktDichloromethaneHCID 6344—
EduktPotassium CarbonateHCID 11430—
Edukt4-Bromo-2-fluorobenzonitrileHCID 736029—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Bromo-2-methoxybenzonitrileHCID 2234670295,6%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

A mixture of 4-bromo-2-fluoro-benzonitrile (15.0 g, 75.0 mmol), methanol (30.4 mL, 350 mmol) and potassium carbonate (31.1 g, 225 mmol) in DMF (150 mL) was stirred under argon at 55° C. overnight. At this point TLC (100% methylene chloride) revealed no starting material, and the reaction mixture was poured into ether (300 mL) and water (150 mL). The layers were separated, and the organic layer was washed with water (150 mL) and brine (50 mL), dried over Mg2SO4, filtrated, and concentrated under reduced pressure, providing (15.2 g, 95.5%) of 4-bromo-2-methoxy-benzonitrile as a white solid. 1H-NMR (CDCl3) δ 7.41 (d, J=8.1 Hz, 1H), 7.16 (dd, J=8.1, 1.6 Hz, 1H), 7.13 (d, J=1.6 Hz, 1H), 3.93 (s, 3H); MS GC-MS (M+=211; RT=6.15 min).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420066B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-dfe0619ae872459c9e0030ceb8e4fcb6
Quellennotizuspto-grants-2008_09