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HRID 413470作成日:2026年10月25日

Ethyl 6-methylnicotinate → 6-Methyl-α-[4-(methylthio)phenyl]-β-oxo-3-pyridinepropanenitrile

https://huagongshe.com/reaction/413470

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 6-methylnicotinateHCID 281994—
反応物2-(4-(Methylthio)phenyl)acetonitrileHCID 2760087—
反応物Sodium MethoxideHCID 10942334—
溶媒TolueneHCID 1140—
生成物6-Methyl-α-[4-(methylthio)phenyl]-β-oxo-3-pyridinepropanenitrileHCID 11300542—

反応手順

Under an atmosphere of nitrogen, a mixture of 38.5 g (250 mmol) of ethyl 6-methylnicotinate, 29.9 g (500 mmol) of sodium methoxide (90.5%) and 300 ml of toluene was added, at 85-90° C. and over the course of 30 min, to a solution of 47.3 g (250 mmol) of 4-(methylthio)phenylacetonitrile in 75 ml of toluene. This mixture was stirred under reflux for 14 h, then distilled until the overhead temperature exceeded 110° C. and kept at reflux for another 6 h. The reaction mixture was poured into 500 g of ice water, the organic phase was decanted off and the aqueous phase was extracted with 3×100 ml of toluene. The aqueous phase was acidified to pH 6.0 using conc. HCl. The resulting yellow-beige suspension was filtered and the residue was washed with water and dried. This gave 53.9 g (76%) of the title product in the form of a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06566527B1
出典データセットuspto-grants-2003_05
ORD IDord-d2fbf46e21984939a9c3ace70bf669b7
出典メモuspto-grants-2003_05