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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335392생성일: 2026년 10월 24일

Potassium Hydroxide → 7-[4-Nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptane

https://huagongshe.com/ko/reaction/335392

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물5-Fluoro-2-nitrobenzotrifluorideHCID 223094—
반응물7-Azabicyclo[2.2.1]heptane hydrochlorideHCID 16279503—
촉매Tetrabutylammonium BromideHCID 74236—
용매DichloromethaneHCID 6344—
생성물7-[4-Nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptaneHCID 57516843—

반응 단계

4-fluoro-1-nitro-2-(trifluoromethyl)benzene was dissolved in 3 vol DCM. Tetrabutylammoniumbromide (0.05 eq) and KOH (50 wt %, 3.6 eq) were added. 7-azabicyclo[2.2.1]heptane hydrochloride (8-HCl) was then added at 0-5° C. The reaction was warmed up to ambient temperature and monitored by HPLC. Once substantially complete, the layers were separated and the organic layer was washed with 1M HCl. The layers were separated and the aqueous layer was discarded. The organic layer was washed once with water, once with brine, and then distilled. The resulting material was recrystallized from cyclohexane at reflux. The solid was filtered, washed with cyclohexane, and dried in a vacuum oven at 45° C. with a N2 gas bleed to provide 7-[4-nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptane (9).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08884018B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-15aba32715384f66828f7e2d969d7239
출처 메모uspto-grants-2014_11