関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl 6-methylnicotinate | HCID 281994 | — |
| 反応物 | 2-(4-(Methylthio)phenyl)acetonitrile | HCID 2760087 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 6-Methyl-α-[4-(methylthio)phenyl]-β-oxo-3-pyridinepropanenitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06566527B1 |
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| 出典データセット | uspto-grants-2003_05 |
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| ORD ID | ord-d2fbf46e21984939a9c3ace70bf669b7 |
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| 出典メモ | uspto-grants-2003_05 |
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