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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359383생성일: 2026년 10월 25일

Sodium Chloride → 4-[2-[2,3-Dihydro-2-(4-fluorophenyl)-2-methyl-3-oxo-5-furanyl]ethenyl]benzonitrile

https://huagongshe.com/reaction/359383

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Sodium HydroxideHCID 14798—
반응물4-CyanobenzaldehydeHCID 66042—
반응물2-(4-Fluorophenyl)-2,5-dimethylfuran-3(2H)-oneHCID 15086704—
용매EthanolHCID 702—
생성물4-[2-[2,3-Dihydro-2-(4-fluorophenyl)-2-methyl-3-oxo-5-furanyl]ethenyl]benzonitrileHCID 5364862638.7%

반응 단계

To a solution of p-cyanobenzaldehyde (1.6 g, 11.8 mM) and 2,5-dimethyl-2-(4-fluorphenyl)-3(2H)-furanone (2.0 g, 9.8 mM) in ethanol (75 mL), was added 1N aqueous sodium hydroxide (1.0 mL, 1 mM). After the reaction solution was stirred at room temperature for two days, saturated aqueous sodium chloride (400 mL) was added. The aqueous layer was extracted with dichloromethane (3×100 mL). The combined dichloromethane extracts were washed with saturated aqueous sodium chloride (50 mL), dried over MgSO4, filtered and concentrated to give an orange liquid. The crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate) to give a yellow crystalline solid (1.2 g, 38% yield), m.p. 140°-142° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05001126
출처 데이터셋uspto-grants-1991_03
ORD IDord-512b3fe8570b43ae928e1f12c97eb2d0
출처 메모uspto-grants-1991_03