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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353049Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/353049

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 0.5 N 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
PatentnummerUS06750214B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-cf4eb2fcce58450c9e5b5f962b9df908
Quellennotizuspto-grants-2004_06