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HRID 1884562생성일: 2026년 10월 27일

Hexane → 1-(3,5-Dichloropyridin-4-yl)-3-methoxymethoxypropane

https://huagongshe.com/reaction/1884562

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물3,5-DichloropyridineHCID 17153—
반응물1-Bromo-3-methoxymethoxypropaneHCID 12709288—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-(3,5-Dichloropyridin-4-yl)-3-methoxymethoxypropaneHCID 2350627613.3%

반응 조건

온도0 °C

반응 단계

3,5-Dichloropyridine (4.4 g, 30 mmol) is dissolved in THF (100 ml), and thereto is added a solution of n-butyl lithium in hexane (19 ml, 30 mmol) at −70° C., and the mixture is stirred for 15 minutes. 1-Bromo-3-methoxymethoxypropane (6.0 g, 33 mmol) is added to the mixture, and the mixture is warmed to 0° C. over a period of time for one hour. The reaction is quenched with a saturated brine (50 ml), and the mixture is extracted with ethyl acetate (150 ml×2). The organic layer is washed with a saturated brine (100 ml×2), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to give 1-(3,5-dichloropyridin-4-yl)-3-methoxymethoxypropane (1.0 g) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06765095B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-95fecb186f3649c6953c9345bb4553df
출처 메모uspto-grants-2004_07