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HRID 1017662作成日:2026年10月27日

Benzeneacetonitrile, 4-fluoro- → 1-(2-Chloropyridin-4-yl)-2-cyano-2-(4-fluorophenyl)ethanone

https://huagongshe.com/reaction/1017662

反応式

関与物質

役割名称HCID仕込み量
反応物Benzeneacetonitrile, 4-fluoro-HCID 68016—
反応物Sodium ethoxideHCID 2723922—
反応物Methyl 2-chloropyridine-4-carboxylateHCID 2736842—
溶媒EthanolHCID 702—
生成物1-(2-Chloropyridin-4-yl)-2-cyano-2-(4-fluorophenyl)ethanoneHCID 22987967—

反応手順

4-Fluorophenylacetonitrile (11.13 g, 82 mmol) was dissolved in absolute ethanol (100 ml) and sodium ethoxide (2wt % in EtOH) (46 ml, 123 mmol) was added in one portion. The resulting brown solution was stirred for 10 min. at room temperature. A solution of 2-chloropyridine-4-carboxylic acid methyl ester (14.1 g, 82 mmol) in absolute ethanol (100 ml) was then added to the reaction over 3-5 min. The reaction mixture was then refluxed for 2 h during which time the color turned to dark brown. The reaction mixture was concentrated in vacuo and water (100 ml) was added to the resulting residue. The pH of the reaction mixture was adjusted to 3 using 10% hydrochloric acid. The product was extracted with ethyl acetate and the combined ethyl acetate extracts were dried over sodium sulfate, filtered and concentrated in vacuo to yield 1-(2-chloropyridin-4-yl)-2-cyano-2-(4-fluorophenyl)ethanone as a dark brown solid which was used without further purification (22.0 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479507B2
出典データセットuspto-grants-2002_11
ORD IDord-c7b6538e8bd04875becf99e38f3dbbe9
出典メモuspto-grants-2002_11