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HRID 1267940作成日:2026年10月25日

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

https://huagongshe.com/reaction/1267940

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物3,5-DichloropyridineHCID 17153—
反応物1-Bromo-3-methoxymethoxypropaneHCID 12709288—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3,5-Dichloropyridin-4-yl)-3-methoxymethoxypropaneHCID 2350627613.3%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06555557B1
出典データセットuspto-grants-2003_04
ORD IDord-d40f298785874965b2dff1cad71ccaad
出典メモuspto-grants-2003_04