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HRID 76097作成日:2026年10月24日

6-Bromo-3,5-dimethoxypicolinonitrile → 6-Ethyl-3,5-dimethoxy-pyridine-2-carbonitrile

https://huagongshe.com/ja/reaction/76097

反応式

関与物質

役割名称HCID仕込み量
反応物6-Bromo-3,5-dimethoxypicolinonitrileHCID 73554911—
反応物HCID 178418443HCID 178418443—
触媒Dichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickelHCID 2724937—
溶媒TetrahydrofuranHCID 8028—
生成物6-Ethyl-3,5-dimethoxy-pyridine-2-carbonitrileHCID 66986777—

反応条件

温度0 °C

反応手順

Impure 6-bromo-3,5-dimethoxy-pyridine-2-carbonitrile (462 mg; <1.9 mmol) was dissolved in tetrahydrofuran (20 mL) under nitrogen, and to the solution was added 1,3-bis(diphenylphosphino)propane nickel (II) chloride (105 mg; 0.19 mmol). The solution was cooled to 0° C., and a solution of ethyl magnesium bromide (1.0 molar in THF; 2.7 mL; 1.4 eq.) was slowly added. The reaction was stirred for five minutes, and quenched with saturated aqueous ammonium chloride (10 mL). To the reaction was added ethyl acetate (40 mL) and water (40 mL). The organic layer was isolated, dried over sodium sulfate, evaporated, and purified by column chromatography to give 6-ethyl-3,5-dimethoxy-pyridine-2-carbonitrile (114 mg; 0.6 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835464B2
出典データセットuspto-grants-2014_09
ORD IDord-532f1d6b6fa349359073f09aec098b3b
出典メモuspto-grants-2014_09