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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359384생성일: 2026년 10월 24일

Sodium Chloride → 2-Methyl-2-(4-fluorophenyl)-5-[2-(2-pyridinyl)ethenyl]-3(2H)-furanone

https://huagongshe.com/ko/reaction/359384

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참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물2-PyridinecarboxaldehydeHCID 14273—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2-(4-Fluorophenyl)-2,5-dimethylfuran-3(2H)-oneHCID 15086704—
용매EthanolHCID 702—
생성물2-Methyl-2-(4-fluorophenyl)-5-[2-(2-pyridinyl)ethenyl]-3(2H)-furanoneHCID 5414433659.4%

반응 조건

온도80 °C

반응 단계

To a solution of 2-pyridinecarboxaldehyde (1.26 g, 10.2 mM) and 2,5-dimethyl-2-(4-fluorophenyl)-3(2H)-furanone (2.0 g, 9.8 mM) in ethanol (100 mL), was added 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 0.2 mL, 1.3 mM). The reaction solution was heated at 80° C. for 4 hours. After the reaction solution cooled to room temperature, saturated aqueous sodium chloride (400 mL) was added. The aqueous layer was extracted with diethyl ether (3×100 mL). The combined ethereal extracts were washed with saturated aqueous sodium chloride (50 mL), dried over MgSO4, filtered and concentrated to give a yellow liquid. The crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate) to yield a yellow solid (1.7 g, 59% yield), m.p. 70°-72° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05001126
출처 데이터셋uspto-grants-1991_03
ORD IDord-c6540c33127b4f3bbe85a15717c2474f
출처 메모uspto-grants-1991_03