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HRID 38081作成日:2026年10月27日

4-Methylpyridine → 1-(3-Methoxyphenyl)-2-(4-pyridyl)ethanone

https://huagongshe.com/reaction/38081

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylpyridineHCID 7963—
反応物Ammonium ChlorideHCID 25517—
反応物Methyl 3-methoxybenzoateHCID 79332—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3-Methoxyphenyl)-2-(4-pyridyl)ethanoneHCID 1127622871.7%

反応手順

To a solution of 4-methyl-pyridine (1.04 mL, 10.74 mmol) in anhydrous tetrahydrofuran (40 mL) at 0° C. a 1 M solution of sodium hexamethyldisilazide in tetrahydrofuran (21.5 mL, 21.5 mmol, 2 eq) was added dropwise and the reaction was stirred for 20 minutes. Neat methyl 3-methoxybenzoate (1.8 g, 10.74 mmol, 1 eq) was then added and the reaction was stirred at 0° C. for one hour. The reaction was poured into saturated ammonium chloride solution and, after basification with saturated aqueous NaHCO3, extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was taken up with n-hexane and filtered to give 1.75 g (72%) of the desired product as beige solid (1.775 g, 50%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524707B2
出典データセットuspto-grants-2013_09
ORD IDord-6d51969d966040b2b5589d90636798f0
出典メモuspto-grants-2013_09