関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nitric Acid | HCID 944 | — |
| 反応物 | 2-Bromo-6-methylpyridine 1-oxide | HCID 3652084 | — |
| 溶媒 | Sulfuric Acid | HCID 1118 | — |
| 生成物 | 2-Bromo-6-methyl-4-nitro-1-oxo-1lambda~5~-pyridine | HCID 2751816 | 57% |
反応手順
To cooled nitric acid (concentrated, 168 ml) was added sulfuric acid (concentrated, 300 ml) under cooling followed by 2-bromo-6-methyl-pyridine 1-oxide (35 g, 0.186 mol). The mixture was stirred at 70° C. for 4 hours, cooled to room temperature and poored slowly on crushed ice. A stream of nitrogen was bubbled through the mixture overnight. The mixture was basified to pH 8 under cooling with NaOH (10N, ca. 1 L), diluted with water (3 L) and extracted with DCM (5×). The combined organic phases were dried (sodium sulfate) and evaporated to dryness to yield 27.6 g of a yellow crystaline solid (0.118 mol, 57%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09321724B2 |
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| 出典データセット | uspto-grants-2016_04 |
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| ORD ID | ord-970edf86b814412faf18b6f7474e2814 |
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| 出典メモ | uspto-grants-2016_04 |
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