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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 478612Erstellt: 25. Oktober 2026

Sodium hydride → 3-(o-Bromobenzyloxy)4-methoxybenzonitrile

https://huagongshe.com/reaction/478612

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt2-Bromobenzyl alcoholHCID 72850—
Edukt3-Fluoro-4-methoxybenzonitrileHCID 2774548—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(o-Bromobenzyloxy)4-methoxybenzonitrileHCID 2270701771,4%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of 2-bromobenzyl alcohol (16.50 g, 88.2 mmol) in DMF (100 ml) was added sodium hydride (60% dispersion in mineral oil, 2.94 g, 73.5 mmol) and this was followed by 3-fluoro-4-methoxybenzonitrile (8.88 g, 58.8 mmol) and the resulting mixture was heated to 90° C. for 2 h under N2. After cooling, the mixture was partitioned between ether and H2O, the organic layer washed sequentially with 0.5N HCl and saturated brine and then dried over MgSO4. Trituration with ether/pentane (1/3, v/v) afforded the subtitle compound as an off-white solid (13.35 g, 71%). Rf 0.27 (hexane/EtOAc 5/1, v/v). MS m/z 318, 320 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06642242B2
Quelldatensatzuspto-grants-2003_11
ORD IDord-37301b24540e494493599c8b813ae6cb
Quellennotizuspto-grants-2003_11