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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359385생성일: 2026년 10월 24일

Sodium Chloride → 2-(4-Fluorophenyl)-2-methyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanone

https://huagongshe.com/ko/reaction/359385

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Sodium HydroxideHCID 14798—
반응물3-ThiophenecarboxaldehydeHCID 68135—
반응물2-(4-Fluorophenyl)-2,5-dimethylfuran-3(2H)-oneHCID 15086704—
용매EthanolHCID 702—
생성물2-(4-Fluorophenyl)-2-methyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanoneHCID 5369929962%

반응 단계

To a solution of 3-thiophenecarboxaldehyde (1.3 g, 1.2 mM) and 2,5-dimethyl-2-(4-fluorophenyl)-3(2H)-furanone (2.0 g, 9.8 mM) in ethanol (75 mL), was added 1N aqueous sodium hydroxide (2 mL, 2 mM). The reaction solution was stirred at room temperature for one day. After 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 a brown oil. The crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate) to afford a yellow solid (1.8 g, 62% yield), m.p. 97°-98° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05001126
출처 데이터셋uspto-grants-1991_03
ORD IDord-86b3919747e04f9683e021ce45808f74
출처 메모uspto-grants-1991_03