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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335391생성일: 2026년 10월 25일

Dimethyl Sulfoxide → 7-[4-Nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptane

https://huagongshe.com/reaction/335391

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Sodium CarbonateHCID 10340—
반응물5-Fluoro-2-nitrobenzotrifluorideHCID 223094—
반응물7-Azabicyclo[2.2.1]heptane hydrochlorideHCID 16279503—
용매Ethyl AcetateHCID 8857—
생성물7-[4-Nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptaneHCID 57516843—

반응 조건

온도55 °C

반응 단계

4-fluoro-1-nitro-2-(trifluoromethyl)benzene (7) (901 g, 4.309 mol) was introduced into a 30 L jacketed vessel along with Na2CO3 (959.1 g, 9.049 mol) and DMSO (5 L, 5.5 vol) under nitrogen atmosphere and stirring. 7-azabicyclo[2.2.1]heptane hydrochloride (8-HCl) (633.4 g, 4.740 mol) was then added to the vessel in portions. The temperature was gradually raised to 55° C. When the reaction was substantially complete, the mixture was diluted with 10 vol EtOAc and washed with water (5.5 vol) three times or until DMSO in the aqueous layer disappeared (HPLC). The organic layer was concentrated to 4 vol and then the solvent was swapped with cyclohexane until all the EtOAc was removed, and the total volume in the flask was about 4 vol containing cyclohexane. The reaction mixture was heated to 60° C. on a rotary evaporator for 30 min. Then the solution was cooled to room temperature with stirring or rotation for 3 h. When all the solid crystallized, the solution was concentrated to dryness 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-72df13e9756240768e5793ce75278fc7
출처 메모uspto-grants-2014_11