参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 反应物 | 碳酸钾 | HCID 11430 | — |
| 反应物 | 高锰酸钾 | HCID 516875 | — |
| 反应物 | 2-乙酰氨基-5-溴-6-甲基吡啶 | HCID 954589 | — |
| 溶剂 | 吡啶 | HCID 1049 | — |
| 产物 | 6-乙酰氨基-3-溴吡啶羧酸 | HCID 25306988 | 603.8% |
反应步骤
To a solution of N-(5-bromo-6-methyl-pyridin-2-yl)-acetamide 48.46 g in pyridine 250 ml was added water 250 ml and the mixture warmed to 90° C. and potassium carbonate 2.2 g was added. Potassium permanganate was added portionwise over 10 h and the mixture allowed to cool slowly overnight. The reaction mixture was re-heated to 90° C. for 2 h, cooled slightly and filtered to remove manganese dioxide. The filtrate was evaporated in vacuo and the residue partitioned between water 1 L and ethyl acetate 500 ml. The aqueous solution was washed with ethyl acetate. The organic solutions were combined, washed with brine, dried MgSO4 and evaporated in vacuo to recover unchanged starting materials 12.6 g. The aqueous solution was acidified with concentrated hydrochloric acid (circa 80 ml) and the solid product filtered off, washed with a minimum of water, sucked dry and then dried at 80° C. (vac) to give 6-acetylamino-3-bromo-pyridine-2-carboxylic acid 24.9 g
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07893077B2 |
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| 来源数据集 | uspto-grants-2011_02 |
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| ORD ID | ord-f06965780ec74d4d9f5a69f09679b26e |
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| 来源说明 | uspto-grants-2011_02 |
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