戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 229354作成日:2026年10月25日

Piperazine → 1-(2-Methoxy-5-methylphenyl)piperazine

https://huagongshe.com/reaction/229354

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物Cesium carbonateHCID 10796—
反応物2-Bromo-4-methylanisoleHCID 89143—
反応物Binap, (A+-)-HCID 634876—
溶媒TolueneHCID 1140—
生成物1-(2-Methoxy-5-methylphenyl)piperazineHCID 1935711567.1%

反応手順

15 mg (0.016 mmol, 0.027 eq) Tris(dibenzylidene-acetone)dipalladium (0) (Pd2dba3), 27 mg (0.043 mmol, 0.072 eq) racemic-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl [(±)-BINAP] and 450 mg (1.38 mmol, 2.3 eq) cesium carbonate were combined in a microwave vial. 1.5 mL anhydrous toluene was added, followed by 121 mg (0.60 mmol, 1.0 eq) 2-bromo-4-methylanisole and 207 mg (2.40 mmol, 4.0 eq) piperazine. The vial was flushed with nitrogen prior to being microwaved at 140° C. for 30 minutes. The reaction mixture was diluted with 3.0 mL DMSO:methanol (1:1), filtered and purified by reverse-phase HPLC (2-99% CH3CN in 0.085% TFA (aq), 50 mL/min, 3×1.5 mL injected). Yield=83 mg (43%) of 1-(2-Methoxy-5-methyl-phenyl)-piperazine as a pale yellow oil (isolated as the mono-TFA salt);

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07563795B2
出典データセットuspto-grants-2009_07
ORD IDord-08d8e89934894921bc0a6c398c241777
出典メモuspto-grants-2009_07