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HRID 72834作成日:2026年10月26日

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

https://huagongshe.com/reaction/72834

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-4-fluorobenzeneHCID 9993—
反応物Sodium HydroxideHCID 14798—
反応物8-Benzyl-8-azabicyclo(3.2.1)octan-3-oneHCID 119846—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物8-Benzyl-3-(4-fluoro-phenyl)-8-aza-bicyclo[3.2.1]octan-3-olHCID 13091227—

反応条件

温度-35 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829027B2
出典データセットuspto-grants-2014_09
ORD IDord-3daac1c55a1b46dd80d595152ab04052
出典メモuspto-grants-2014_09