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HRID 65038作成日:2026年10月24日

Water → 1-(4-Methoxyphenyl)-2-(pyridin-3-yl)ethanone

https://huagongshe.com/ja/reaction/65038

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-MethylpyridineHCID 7970—
反応物TetrahydrofuranHCID 8028—
反応物HexaneHCID 8058—
反応物ButyllithiumHCID 178418339—
溶媒DiisopropylamineHCID 7912—
生成物1-(4-Methoxyphenyl)-2-(pyridin-3-yl)ethanoneHCID 23835185%

反応条件

温度-78 °C

反応手順

In 300 ml of anhydrous tetrahydrofuran was dissolved 33.2 ml of diisopropylamine, and the solution was cooled to -78° C., to which was added dropwise, while stirring, 148 ml of hexane solution of n-butyl lithium (1.6 M). The mixture was stirred for further 10 minutes at the same temperature, followed by dropwise addition of 20 g of β-picoline. The temperature was then raised up to -10°-0° C. and the mixture was stirred for 20 minutes, to which was added dropwise 19.4 g of ethyl p-anisole dissolved in 40 ml of anhydrous tetrahydrofuran. Then, the mixture was stirred for one hour at room temperature, followed by addition of about 100 ml of water. The organic solvent was evaporated off, and the concentrated solution was subjected to extraction with ethyl acetate. The extract solution was washed with water and dried on magnesium sulfate, followed by crystalliation from a mixture of ethyl acetate-isopropylether to give 20.8 g (yield: 85%) of 1-(4-methoxyphenyl)-2-(3-pyridyl)-ethanone, m.p. 71°-72° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04612321
出典データセットuspto-grants-1986_09
ORD IDord-1cd4ccb5bc3a45e2ab408c62b1b1f9ac
出典メモuspto-grants-1986_09