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(4,5-Dimethylfuran-2-yl)-(4-methyl-pyridin-2-yl)-methanol → (4,5-Dimethylfuran-2-yl)-(4-methyl-pyridin-2-yl)-methanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (4,5-Dimethylfuran-2-yl)-(4-methyl-pyridin-2-yl)-methanol | HCID 23078475 | — |
| 触媒 | HCID 178418406 | HCID 178418406 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | (4,5-Dimethylfuran-2-yl)-(4-methyl-pyridin-2-yl)-methanone | HCID 23078347 | 77.4% |
反応手順
(4,5-Dimethylfuran-2-yl)-(4-methyl-pyridin-2-yl)-methanol (900 mg) was dissolved in chloroform (20 ml) to prepare a solution. Manganese dioxide (3.6 g) was added to the solution, and the mixture was stirred at room temperature overnight. Further, manganese dioxide (1.8 g) was then added to the reaction solution, and the mixture was stirred at room temperature for 5 hr. The reaction solution was filtered through Celite, and the solvent was removed from the filtrate by distillation under the reduced pressure, and the residue was purified by column chromatography using hexane-ethyl acetate to give (4,5-dimethylfuran-2-yl)-(4-methyl-pyridin-2-yl)-methanone (690 mg, yield 77%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07560558B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-b79a5c0abf3748e197e2d1d621430bd9 |
| 出典メモ | uspto-grants-2009_07 |