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HRID 256578作成日:2026年10月26日

Benzene, 1-fluoro-2-(trifluoromethyl)- → 3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octane

https://huagongshe.com/reaction/256578

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 1-fluoro-2-(trifluoromethyl)-HCID 9807—
反応物(+-)-3-QuinuclidinolHCID 15381—
反応物Sodium hydrideHCID 24758—
溶媒DimethylformamideHCID 6228—
生成物3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octaneHCID 1019933379%

反応条件

温度70 °C

反応手順

A solution of 1.78 g (14 mmol) of 3-quinuclidinol in 20 ml of dry N,N-dimethylformamide (DMF) was added dropwise under nitrogen to a suspension of 0.6 g (15 mmol) of sodium hydride in 20 ml of dry DMF. The mixture was stirred for 15 min at 70° C., and a solution of 3.8 ml (30 mmol) of 2-fluoro-(trifluoromethyl)benzene in 8 ml of dry DMF was added dropwise. The mixture was stirred for another 1.5 h, after which the solvent was evaporated. The residue was dissolved in ethyl acetate and washed with brine. The ethyl acetate layer was separated, dried over magnesium sulfate and evaporated to dryness. The crude compound was purified by column chromatography on silica using methanol-dichloromethane (2:8) as eluent to give 3.0 g (59% yield) of 3-[2-(trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2 ]octane, which was converted into the oxalate salt by treatment with oxalic acid and recrystallization from methanol. m.p. 174° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05258392
出典データセットuspto-grants-1993_11
ORD IDord-ec0a81e2fdd044d89fb54e6141d93b73
出典メモuspto-grants-1993_11