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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52485생성일: 2026년 10월 24일

Imidazole → 2-Phthalimidomethyltetrahydroquinoline

https://huagongshe.com/ko/reaction/52485

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참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물IodineHCID 807—
반응물TriphenylphosphineHCID 11776—
반응물Sodium ThiosulfateHCID 24477—
반응물(1,2,3,4-Tetrahydroquinolin-2-yl)methanolHCID 15052240—
반응물Phthalimide potassium saltHCID 24194345—
용매WaterHCID 962—
용매Acetonitrile tolueneHCID 21584213—
생성물2-PhthalimidomethyltetrahydroquinolineHCID 1010838475%

반응 조건

온도0 °C

반응 단계

To a solution of 2-hydroxymethyltetrahydroquinoline (10 g, 61 mmol), imidazole (10.0 g, 147 mmol), and triphenylphosphine (19.0 g, 72.4 mmol) in a mixed solvent of 5:1 toluene/acetonitrile (360 mL) was added iodine (16.85 g, 66.4 mmol) at 0° C. The mixture was stirred for 2 h at 0° C. and aqueous sodium thiosulfate was added. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and concentrated. The residue was triturated with diethyl ether and insoluble materials were removed by filtration. The filtrate was concentrated and the residue was dissolved in DMF (60 mL) and potassium phthalimide (13.6 g, 73.48 mmol) was added. The mixture was heated at 60° C. for 2 h and diluted with water (200 mL). The mixture was extracted with 1:1 toluene/ethyl acetate (200 mL×2). The organic layers were washed with brine, dried over magnesium sulfate, and concentrated. The residue was purified with silica gel column chromatography with 10:1 to 6:1 hexane/ethyl acetate to give 10.25 g of 2-Phthalimidomethyltetrahydroquinoline (75%): 1H NMR (270 MHz, CDCl3) δ7.86 (m, 2H), 7.74 (m, 2H), 6.95 (m, 2H), 6.59 (t, 1H, J=8 Hz), 6.49 (d, 1H, J=8 Hz), 3.91 (dd, 1H, J=14, 5 Hz), 3.78 (dd, 1H, J=14, 5 Hz), 3.68 (m, 1H), 2.78 (m, 2H), 2.00 (m, 1H), 1.69 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616586
출처 데이터셋uspto-grants-1997_04
ORD IDord-c19ff97047444c78a2471782a2f7d364
출처 메모uspto-grants-1997_04