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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 337120Erstellt: 25. Oktober 2026

Benzyl Alcohol → 3-Fluoro-2-(phenylmethoxy)benzonitrile

https://huagongshe.com/reaction/337120

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl AlcoholHCID 244—
EduktSodium hydrideHCID 24758—
Edukt2,3-DifluorobenzonitrileHCID 88935—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Fluoro-2-(phenylmethoxy)benzonitrileHCID 57705211—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

Benzyl alcohol (5.51 mL) was added dropwise over 20 min to a stirred suspension of sodium hydride (2.128 g of a 60% dispersion in mineral oil) and 2,3-difluorobenzonitrile (7.4 g) in THF (100 mL) with external ice bath cooling to maintain temperature around 25° C. After addition was complete, the reaction mixture was stirred at room temperature for 24 h, quenched with water (200 mL) and extracted into ethyl acetate (3×120 mL), combined organics were dried (MgSO4) and evaporated. The residual oil was purified (SiO2 chromatography eluting with 20% ether in isohexane) to give the subtitle compound as an oil (9.70 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889692B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-f120ff53d87e4cdfb8c54600fef750b8
Quellennotizuspto-grants-2014_11