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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322955생성일: 2026년 10월 25일

3-Pyridinemethanol → 2-Fluoro-4-(3-pyridylmethoxy)benzonitrile

https://huagongshe.com/reaction/322955

반응식

참여 물질

역할이름HCID투입량
반응물3-PyridinemethanolHCID 7510—
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물2-Fluoro-4-hydroxybenzonitrileHCID 2734675—
용매TetrahydrofuranHCID 8028—
생성물2-Fluoro-4-(3-pyridylmethoxy)benzonitrileHCID 2201049885.8%

반응 조건

온도0 °C

반응 단계

A solution of triphenylphosphine (20 g) in tetrahydrofuran (300 mL) cooled at 0° C. is treated dropwise during 5 minutes with diisopropyl azodicarboxylate (15 mL) and stirred for 15 minutes at 0° C. It is then treated, dropwise, with a solution of 2-fluoro-4-hydroxybenzonitrile (7 g) and 3-pyridylmethanol (7 g) in tetrahydrofuran (200 mL) during 2 hours, and stirring is continued at ambient temperature for 18 hours. The mixture is concentrated in vacuo and the residue is dissolved in ethyl acetate (500 mL) and the solution is washed with hydrochloric acid (3×100 mL; 1 N) and the remaining organic layer is discarded. The combined acid washings are basified to pH 10 by treatment with solid sodium hydroxide and extracted with ethyl acetate (3×100 mL). This organic extract is dried over magnesium sulphate and concentrated in vacuo, and the residue is recrystallized from isopropyl ether, to give 2-fluoro-4-(3-pyridylmethoxy)benzonitrile (10 g), in the form of a white solid, m.p. 105-110° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211234B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-42b8e82bbf504197909a95a868915cbe
출처 메모uspto-grants-2001_04