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HRID 1961688作成日:2026年10月25日

Piperazine → 1-(2-Chloro-4-fluorophenyl)piperazine

https://huagongshe.com/reaction/1961688

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物Binap, (A+-)-HCID 634876—
反応物1-Bromo-2-chloro-4-fluorobenzeneHCID 2733406—
反応物Sodium t-butoxideHCID 23676156—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物1-(2-Chloro-4-fluorophenyl)piperazineHCID 18423151—

反応条件

温度120 °C

反応手順

A suspension of 1-bromo-2-chloro-4-fluorobenzene (4.19 g, 20 mmoles), piperazine (10.32 g, 120 mmoles), sodium tert-butoxide (2.3 g, 1.5 mmoles), tris(dibenzylideneacetone)dipalladium (366 mg, 0.4 mmoles) and racemic (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (747 mg, 1.2 mmoles) in toluene (2 mL) was heated to 120° C. overnight. The mixture was cooled, filtered and the filtrate concentrated under reduced pressure. The crude residue was purified by column chromatography (silica gel, 0-5% 2N methanolic ammonia in DCM) to provide the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415354B2
出典データセットuspto-grants-2013_04
ORD IDord-7f1f298730794705b9f359e2797fc3d4
出典メモuspto-grants-2013_04