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2-Nitroacetamide → 2(1H)-Pyridinone, 5-ethyl-6-methyl-3-nitro-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Nitroacetamide | HCID 279256 | — |
| 反応物 | Piperidinium acetate | HCID 3014295 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | 2-Ethyl-3-oxobutanal | HCID 15228410 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2(1H)-Pyridinone, 5-ethyl-6-methyl-3-nitro- | HCID 10352314 | 80% |
反応手順
A mixture of 2-ethyl-3-oxobutanal, sodium salt (7.5 g, 55 mmol), nitroacetamide (6.6 g, 63 mmol), aqueous piperidinium acetate (4.4 mL) [prepared from glacial acetic acid (42 mL), water (100 mL) and piperidine (72 mL)] in water (45 mL) was stirred at room temperature for 22 hours. The yellow precipitate was collected by filtration and air dried to yield 8.0 g (80%) of 5-ethyl-6-methyl-3-nitro-2-(1H)-pyridinone.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05308854 |
| 出典データセット | uspto-grants-1994_05 |
| ORD ID | ord-e763b5b7379b4dc9a4bb699f2714a2a5 |
| 出典メモ | uspto-grants-1994_05 |