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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33086생성일: 2026년 10월 24일

p-Fluoronitrobenzene → N-(4-nitrophenyl)-N-(2-pyrid-3-ylethyl)amine

https://huagongshe.com/ko/reaction/33086

반응식

참여 물질

역할이름HCID투입량
반응물p-FluoronitrobenzeneHCID 9590—
반응물Potassium CarbonateHCID 11430—
반응물2-(Pyridin-3-yl)ethan-1-amineHCID 854051—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물N-(4-nitrophenyl)-N-(2-pyrid-3-ylethyl)amineHCID 2310483792.8%

반응 조건

온도60 °C

반응 단계

2 g of 4-fluoronitrobenzene, 2.07 g of 2-(3-pyridyl)ethylamine, and 2.35 g of K2CO3 were added to a solution of 20 ml of N-methylpyrrolidinone. The reaction medium was heated at 60° C. for 16 hours and, after cooling to room temperature, was then poured into a water+ice mixture. The yellow precipitate formed was filtered off, reslurried in water, and then dried over P2O5. 3.2 g of N-(4-nitrophenyl)-N-(2-pyrid-3-ylethyl)amine (3) were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429278B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-7a84c7f876da493c8419e1d65ad26d6e
출처 메모uspto-grants-2008_09