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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1357482생성일: 2026년 10월 25일

Water → Piperidine, 1-(4-nitrophenyl)-

https://huagongshe.com/reaction/1357482

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PiperidineHCID 8082—
반응물Potassium CarbonateHCID 11430—
반응물1-Bromo-4-nitrobenzeneHCID 11466—
용매Dimethyl SulfoxideHCID 679—
생성물Piperidine, 1-(4-nitrophenyl)-HCID 81049—

반응 조건

온도100 °C

반응 단계

0.202 g (1.0 mmol) of 1-bromo-4-nitrobenzene and 0.20 ml of piperidine (2.0 mmol) were dissolved in 3 ml of dimethylsulfoxide. 0.207 g (1.5 mmol) of potassium carbonate was added and the reaction mixture was heated to 100° C. After 2 h 100 ml of water was added, and the mixture was extracted a few times with dichloromethane. The combined organic layers were dried over sodium sulfate and evaporated to obtain crude 4-(piperidin-1-yl)-1-nitrobenzene. Following the procedure outlined in Step 2 of Example 1, but substituting 4-piperidin-1-yl-1-nitrobenzene for 1-methyl-4-(4-nitrophenyl)piperazine, afforded 4-piperidin-1-ylaniline, which was reacted with 9-chloroacridine (according to Step 4 in the procedure of Example 1) to obtain the title compound with 6% overall yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06593324B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-d68a9c15e9724614803bb525ca25fa79
출처 메모uspto-grants-2003_07