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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71생성일: 2026년 10월 23일

1-Acetylpiperazine → 1-[4-(2-Methyl-3-nitrophenyl)piperazin-1-yl]ethanone

https://huagongshe.com/ko/reaction/71

반응식

참여 물질

역할이름HCID투입량
반응물1-AcetylpiperazineHCID 83795—
반응물2-Bromo-6-nitrotolueneHCID 123537—
시약Cesium carbonateHCID 10796—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Palladium (II) acetateHCID 4144353—
용매TolueneHCID 1140—
생성물1-[4-(2-Methyl-3-nitrophenyl)piperazin-1-yl]ethanoneHCID 6859297798.46%

반응 조건

온도100 °C

반응 단계

1-bromo-2-methyl-3-nitrobenzene (500 mg, 2.31 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (201 mg, 0.35 mmol) and cesium carbonate (1131 mg, 3.47 mmol) and diacetoxypalladium (52.0 mg, 0.23 mmol) were dissolved in toluene (10 mL) and sealed into a microwave tube degazed and purged with argon. The reaction was heated to 100 °C, over a period of 12 hours. The reaction mixture was cooled down to room temperature, filtered and the residue was evaporated. The crude product was purified by flash chromatography on silica gel eluting with 0 to 10% methanol in dichloromethane. The solvent was evaporated to dryness to afford 1-(4-(2-methyl-3-nitrophenyl)piperazin-1-yl)ethanone (600 mg, 98 %) as a solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-57be3c43ca2f40d482cab5a1bd42b5d5
출처 메모750 AstraZeneca ELN dataset