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HRID 322955作成日:2026年10月26日

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

https://huagongshe.com/reaction/322955

反応式

関与物質

役割名称HCID仕込み量
反応物3-PyridinemethanolHCID 7510—
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
反応物2-Fluoro-4-hydroxybenzonitrileHCID 2734675—
溶媒TetrahydrofuranHCID 8028—
生成物2-Fluoro-4-(3-pyridylmethoxy)benzonitrileHCID 2201049885.8%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211234B1
出典データセットuspto-grants-2001_04
ORD IDord-42b8e82bbf504197909a95a868915cbe
出典メモuspto-grants-2001_04