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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1896111생성일: 2026년 10월 26일

Potassium Carbonate → 2-(4-Benzyl-1-(5-methoxy-2-nitrophenyl)piperazin-2-yl)acetic acid

https://huagongshe.com/reaction/1896111

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물18-Crown-6HCID 28557—
반응물3-Fluoro-4-nitroanisoleHCID 565654—
반응물2-Piperazineacetic acid, 4-(phenylmethyl)-, methyl esterHCID 15665466—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물2-(4-Benzyl-1-(5-methoxy-2-nitrophenyl)piperazin-2-yl)acetic acidHCID 66769807—

반응 조건

온도90 °C

반응 단계

To a solution of Example 12C (0.907 g, 3.65 mmol) in acetonitrile (11.69 mL) was added 2-fluoro-4-methoxy-1-nitrobenzene (0.50 g, 2.92 mmol) and potassium carbonate (2.019 g, 14.61 mmol) in water (2.92 mL) followed by 18-crown-6 (0.039 g, 0.146 mmol), and the mixture was heated with an oil bath at 90° C. (reflux) for 24 hours. The solvent was evaporated and water was added followed by dichloromethane. The water phase was washed three times with dichloromethane to remove starting material and then acidified with 1 N HCl until pH=1. The acid product was extracted three times with dichloromethane, dried quickly with sodium sulfate and concentrated to give the title compound. MS (ESI) m/z 386.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08518933B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-9880190aec6b457b8577ae8afd55e028
출처 메모uspto-grants-2013_08