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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8395생성일: 2026년 10월 23일

Sodium Chloride → 2-[2-(4-Fluorophenyl)ethenyl]-5-fluorobenzonitrile

https://huagongshe.com/ko/reaction/8395

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Sodium hydrideHCID 24758—
반응물4-FluorobenzaldehydeHCID 68023—
반응물HCID 178418744HCID 178418744—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-[2-(4-Fluorophenyl)ethenyl]-5-fluorobenzonitrileHCID 5412512223.2%

반응 단계

Sodium hydride (60% in mineral oil; 1.66 g [0.993 g NaH], 1.4 mmol, 1.10 equiv) was added to a solution of diethyl-2-cyano-4-fluorobenzyl phosphonate (10.2 g-equiv, 37.6 mmol, 1.0 equiv) in DMF (40 mL) over a period of 2 min. The reaction was stirred for 20 min at room temperature. 4-Fluorobenzaldehyde (4.67 g, 38 mmol, 1.0 equiv) was then added over a period of 2 min. After stirring for 18 h, H2O (200 mL) and satd. NaCl (50 mL) were added and the resulting mixture was extracted with EtOAc (2×100 mL). The combined organic layers were washed with 1N NaOH (1×100 mL) and H2O (2×100 mL), dried (anhyd. Na2SO4), and rotary evaporated (>100° C., heat gun). The crude, dark-red crystalline/oil (7.49 g, 82.7%) was chromatographed twice on silica gel (50×250 mm, dry pack), eluting first with hexane/EtOAc [4:1] and the second chromatography with [30:1] to provide a TLC-pure, yellow compound (2.1 g, 23.2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087765B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b1ca4ad206c7491da2afea1c84001543
출처 메모uspto-grants-2006_08