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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1648812생성일: 2026년 10월 25일

2-[2-nitro-4-(trifluoromethyl)phenyl]-1H-benz[de]isoquinoline-1,3(2H)-dione → 11-(trifluoromethyl)-7H-benzimidazo[2,1-a]benz[de]isoquinoline-7-one

https://huagongshe.com/reaction/1648812

반응식

참여 물질

역할이름HCID투입량
반응물2-[2-nitro-4-(trifluoromethyl)phenyl]-1H-benz[de]isoquinoline-1,3(2H)-dioneHCID 20199012—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매Acetic AcidHCID 176—
생성물11-(trifluoromethyl)-7H-benzimidazo[2,1-a]benz[de]isoquinoline-7-oneHCID 1320618359%

반응 단계

2-[2-nitro-4-(trifluoromethyl)phenyl]-1H-benz[de]isoquinoline-1,3(2H)-dione, 134.3 g. (0.347 m.), was hydrogenated at 55° C. in 600 ml. of glacial acetic acid with 15 g. of palladium-on-carbon (5 percent) at 60 psi. The temperature rose to about 100° C., and after 1.5 hours, three equivalents of hydrogen were absorbed with the temperature returning to room temperature. The reaction mixture was heated to boiling and filtered to remove the catalyst. Upon cooling, the precipitated product was collected and washed with 2B ethanol. Recrystallization from N,N-dimethylformamide yielded about 69.2 g. (59 percent yield) of 11-(trifluoromethyl)-7H-benzimidazo[2,1-a]benz[de]isoquinoline-7-one, m.p. about 212°-214° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04413126
출처 데이터셋uspto-grants-1983_11
ORD IDord-978f1a0acc9a45df827a3e61d5bfc742
출처 메모uspto-grants-1983_11