Tetrahydrofuran → 8-Fluoro-6-nitro-1,2,3,4-tetrahydroquinoline
반응식
[F:1][C:2]1[CH:3]=[C:4]([N+:13]([O-:15])=[O:14])[CH:5]=[C:6]2[C:11]=1[NH:10][C:9](=O)[CH2:8][CH2:7]2.C1COCC1>>[F:1][C:2]1[CH:3]=[C:4]([N+:13]([O-:15])=[O:14])[CH:5]=[C:6]2[C:11]=1[NH:10][CH2:9][CH2:8][CH2:7]2참가 물질
3
반응 조건
- 온도
- 60 °C
실험 절차
8-Fluoro-6-nitro-3,4-dihydroquinolin-2(1H)-one (5.9 g, 28.1 mmol) was stirred in borane-THF complex, 1M in THF (140 ml, 140 mmol). The solution was heated to 60° C. and stirred overnight. The mixture was then cooled in an ice bath and quenched via addition of methanol (30 mL). The quenched solution was concentrated, then dissolved in methanol and refluxed for 1 h. The solution was then concentrated onto silica gel and chromatographed using 5-30% ethyl acetate in hexanes to give the desired 8-fluoro-6-nitro-1,2,3,4-tetrahydroquinoline (4.34 g, 22.12 mmol, 79% yield). 1H NMR (DMSO-d6) δ 7.77-7.71 (m, 1H), 7.73 (m, 1H), 7.31 (brs, 1H), 3.35-3.28 (m, 2H), 2.77 (t, J=6.2 Hz, 2H), 1.85-1.77 (m, 2H).
후처리
- temperatureThe mixture was then cooled in an ice bath
- customquenched via addition of methanol (30 mL)
- concentrationThe quenched solution was concentrated
- dissolutiondissolved in methanol
- temperaturerefluxed for 1 h
- concentrationThe solution was then concentrated onto silica gel
- customchromatographed
출처 및 근거
- ORD 기록
- ord-904c2d76e18c423cba4b819bd189807b
- 출처 데이터셋
- uspto-grants-2012_05
- 특허 번호
- US08173813B2
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