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HRID 199作成日:2026年10月23日

Piperazine → 1-(4-Benzyloxy-3-fluorophenyl)piperazine

https://huagongshe.com/ja/reaction/199

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物1-(Benzyloxy)-4-bromo-2-fluorobenzeneHCID 18757491—
試薬Sodium t-butoxideHCID 23676156—
触媒Binap, (A+-)-HCID 634876—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物1-(4-Benzyloxy-3-fluorophenyl)piperazineHCID 2311148371.64%

反応条件

温度110 °C

反応手順

sodium 2-methylpropan-2-olate (6.43 g, 66.88 mmol) was added to 1-(benzyloxy)-4-bromo-2-fluorobenzene (13.43 g, 47.77 mmol) and piperazine (24.69 g, 286.64 mmol) in toluene (140 mL). The resulting mixture was bubbled with nitrogen for 10 minutes then 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (2.97 g, 4.78 mmol) and TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (1.094 g, 1.19 mmol) were added and the mixture was stirred at 110 °C for 20 hours. The reaction mixture was cooled to room temperature then fitered through celite and the filter cake washed with ethyl acetate (500 mL). The filtrate was evaporated to give crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% MeOH in DCM. Pure fractions were evaporated to dryness to afford 1-(4-(benzyloxy)-3-fluorophenyl)piperazine (9.80 g, 71.6 %) as a solid.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-996b98cdf02a43a3b340c4e4f981f563
出典メモ750 AstraZeneca ELN dataset