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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72834Generated: October 27, 2026

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

https://huagongshe.com/reaction/72834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantSodium HydroxideHCID 14798—
Reactant8-Benzyl-8-azabicyclo(3.2.1)octan-3-oneHCID 119846—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product8-Benzyl-3-(4-fluoro-phenyl)-8-aza-bicyclo[3.2.1]octan-3-olHCID 13091227—

Reaction Conditions

Temperature-35 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829027B2
Source datasetuspto-grants-2014_09
ORD IDord-3daac1c55a1b46dd80d595152ab04052
Source noteuspto-grants-2014_09