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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429199생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/429199

반응식

참여 물질

역할이름HCID투입량
반응물Benzeneacetonitrile, 4-fluoro-HCID 68016—
반응물Sodium ethoxideHCID 2723922—
반응물Methyl 2-chloropyridine-4-carboxylateHCID 2736842—
용매EthanolHCID 702—
생성물1-(2-Chloropyridin-4-yl)-2-cyano-2-(4-fluorophenyl)ethanoneHCID 22987967—

반응 단계

4-Fluorophenylacetonitrile (11.13 g, 82 mmol) was dissolved in absolute ethanol (100 ml) and sodium ethoxide (21wt % 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06316464B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-78c5c72b635b4fbba12366730d7605f1
출처 메모uspto-grants-2001_11