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HRID 1366822生成日期:2026年10月23日

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 6-乙酰氨基-3-溴吡啶羧酸

https://huagongshe.com/zh-CN/reaction/1366822

反应方程式

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 25306988603.8%

反应条件

温度90 °C

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

DOI10.6084/m9.figshare.5104873.v1
专利号US07893077B2
来源数据集uspto-grants-2011_02
ORD IDord-f06965780ec74d4d9f5a69f09679b26e
来源说明uspto-grants-2011_02