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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351601생성일: 2026년 10월 25일

2-Quinolinecarboxaldehyde → 2-Quinolinemethanol

https://huagongshe.com/reaction/351601

반응식

참여 물질

역할이름HCID투입량
반응물2-QuinolinecarboxaldehydeHCID 79619—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
생성물2-QuinolinemethanolHCID 73196—
생성물(1,2,3,4-Tetrahydroquinolin-2-yl)methanolHCID 15052240—

반응 단계

Sodium borohydride (21.7 g, 0.57 mol) was added in portions to a solution of quinoline-2-carboxaldehyde (30 g, 0.191 mol) in ethanol (300 mL) at 0° C. The reaction mixture was warmed to room temperature, stirred at room temperature for 2 hrs, and quenched by water. Volatiles were removed under reduced pressure and the residue dissolved in ethyl acetate, washed with water and saturated aqueous sodium chloride, dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel chromatography. Fractions containing product were combined and concentrated under reduced pressure to provide the desired compound and 2-(hydroxymethyl)quinoline. A solution of the recovered 2-(hydroxymethyl)quinoline in ethanol (250 mL) and tetrahydrofuran (250 mL) was hydrogenated at 60 psi in the presence of 5% platinum on carbon at 40° C. for 48 hours. The reaction mixture was filtered and the filtrate concentrated under reduced pressure to provide the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743785B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-f6f7b93775e143ccb92bc7a447b47d8b
출처 메모uspto-grants-2004_06