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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349975생성일: 2026년 10월 25일

Water → 2-(2-Quinolylmethoxy)-5-pyridylmethanol

https://huagongshe.com/reaction/349975

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물2-QuinolinemethanolHCID 73196—
반응물Methyl 6-chloropyridine-3-carboxylateHCID 254249—
용매DimethylformamideHCID 6228—
생성물2-(2-Quinolylmethoxy)-5-pyridylmethanolHCID 2241358050.5%

반응 단계

Sodium hydride (60%, oily, 1.58 g) was added to a solution of 2-quinolylmethanol (6.29 g) and methyl 6-chloro-3-pyridinecarboxylate (6.78 g) in N,N-dimethylformamide (100 ml) at 0° C., and the mixture was stirred for 1 hour. The reaction mixture was poured into water, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and concentrated. Lithium aluminium hydride (1.50 g) was added to a solution of the residue in tetrahydrofuran (150 ml) at 0° C., which was stirred at room temperature for 10 minutes. Sodium sulfate decahydrate (12.7 g) was added to the reaction mixture, which was stirred at room temperature for 1 hour. The precipitate was removed by filtration, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography to obtain 2-(2-quinolylmethoxy)-5-pyridylmethanol (5.31 g, yield 50%) as colorless crystals from the fraction eluted with ethyl acetate. This was recrystallized from ethyl acetate-hexane. Melting point: 124–125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179823B1
출처 데이터셋uspto-grants-2007_02
ORD IDord-6411bf0a3b694b63b90316b29ea63965
출처 메모uspto-grants-2007_02