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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493739생성일: 2026년 10월 25일

7-Methylquinoline → 7-Methyl-2-phenylquinoline

https://huagongshe.com/reaction/493739

반응식

참여 물질

역할이름HCID투입량
반응물7-MethylquinolineHCID 11927—
반응물HCID 178506676HCID 178506676—
용매TetrahydrofuranHCID 8028—
생성물7-Methyl-2-phenylquinolineHCID 287715—

반응 단계

To a solution of 7-methylquinoline (1.63 g, 11.4 mmol) in dry THF (10 mL), cooled by ice/water, is added phenyllithium (1.9M in cyclohexane/ether 70/30, 6.0 mL, 11.4 mmol) dropwise over 5 min. After 15 min, the cooling bath is removed, and the solution is stirred at rt for 5 h. The reaction is quenched by adding MeOH, and stirring is continued overnight. Water is added, the mixture is extracted with EtOAc (3×35 mL), and the combined extracts are dried over MgSO4. The drying agent is filtered off, and air is bubbled into the solution for 7 d. The solvent is evaporated; the residue is dissolved in warm (≈50° C.) EtOAc/hexanes and filtered warm. The filtrate is concentrated and dried in vacuo to obtain the crude title compound that is used directly for the next step. Further purification is possible by chromatography on silica gel (Jones Flashmaster, eluting with hexanes: EtOAc 3:1→2:1→1:1). 1H NMR(CDCl3, 400MHz) δ 2.58 (s, 3H), 7.31 (d, J=3.7 Hz, 1H), 7.36-7.49 (m, 1H), 7.52 (t, J=8.0 Hz, 2H), 7.72 (d, J=8.2 Hz, 1H), 7.82 (d, J=8.2 Hz, 1H), 7.96 (s, 1H), 8.16 (t, J=8.0 Hz, 2H). MS (ES+): m/z 220.3 (100) [MH+]. HPLC: tR=2.7 min (Platform II, nonpolar—5 min).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534797B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-9734af9e2fde42f58e026b25a5b80198
출처 메모uspto-grants-2009_05