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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 505019생성일: 2026년 10월 24일

Formaldehyde → 5-methyl-2,3,3a,4,5,9b-hexahydro-1H-cyclopenta[c]quinoline

https://huagongshe.com/ko/reaction/505019

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물N-MethylanilineHCID 7515—
반응물Boron trifluoride etherateHCID 8000—
반응물CyclopenteneHCID 8882—
반응물Sodium HydroxideHCID 14798—
용매AcetonitrileHCID 6342—
생성물5-methyl-2,3,3a,4,5,9b-hexahydro-1H-cyclopenta[c]quinolineHCID 374370557.7%

반응 조건

온도1.5 °C

반응 단계

N-methyl aniline (1.07 g, 10.0 mmol) was dissolved in 23 ml acetonitrile under N2 atmosphere. Cyclopentene (4.08 g, 60.0 mmol) and paraformaldehyde (300 mg, 10.0 mmol) were added in one portion. The mixture was cooled to 1.5° C. and BF3.OEt2 (3.55 g, 25.0 mmol) was added over a period of 2 minutes. The cooling bath was removed after addition was completed (reaction temp=9° C.). The reaction was completed after 2 hours (HPLC). NaOH (10.5 g in 20 ml water) was added and the mixture stirred overnight. Layers were separated. An inorganic solid was separated by filtration and the organic layer was extracted with ethyl acetate 3×10 ml. The combined organic layers were washed with brine and dried over MgSO4. Evaporation of solvent and flash-chromatography with heptane/ethyl acetate gave 5-Methyl-2,3,3a,4,5,9b-hexahydro-1H-cyclopenta[c]quinoline (1.08 g, 57% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07781427B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-47ec983ca27e4a8f8febbe18aa5c5fba
출처 메모uspto-grants-2010_08