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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72834Erstellt: 24. Oktober 2026

1-Bromo-4-fluorobenzene → 8-Benzyl-3-(4-fluoro-phenyl)-8-aza-bicyclo[3.2.1]octan-3-ol

https://huagongshe.com/de/reaction/72834

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-4-fluorobenzeneHCID 9993—
EduktSodium HydroxideHCID 14798—
Edukt8-Benzyl-8-azabicyclo(3.2.1)octan-3-oneHCID 119846—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
Produkt8-Benzyl-3-(4-fluoro-phenyl)-8-aza-bicyclo[3.2.1]octan-3-olHCID 13091227—

Reaktionsbedingungen

Temperatur-35 °C

Reaktionsschritte

1-Bromo-4-fluoro-benzene (22.7 g) dissolved in diethylether (100 mL) is added to a solution of n-butyllithium (1.7 mol/L in pentane, 86.8 mL) in diethylether (200 mL) cooled to −35° C. The combined solutions are stirred at −35 to −40° C. for 1 h, before 8-benzyl-8-aza-bicyclo[3.2.1]octan-3-one (22.5 g) dissolved in diethylether (150 mL) is added quickly. The solution is warmed to −10° C. within 1 h and then the reaction is quenched by the addition of aqueous NH4Cl solution. The resulting mixture is extracted with ethyl acetate, the combined extracts are washed with brine, and 4 M hydrochloric acid is added to the organic phase. The organic phase is separated from the aqueous phase and an oily precipitation formed after the addition. The oily and aqueous phase are combined and basified with 4 M aqueous NaOH solution and the resulting mixture is extracted with ethyl acetate. The organic extracts are dried (Na2SO4) and the solvent is evaporated to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829027B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-3daac1c55a1b46dd80d595152ab04052
Quellennotizuspto-grants-2014_09