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A two-step continuous flow synthesis of 4-nitropyridine

机译:两步连续流式合成4-硝基吡啶

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摘要

4-Nitropyridine, a key intermediate in medicinal products, was successfully prepared from pyridine N-oxide in a two-step -approach. Pyridine N-oxide was nitrated with HNO3 and H2SO4 to give 4-nitropyridine N-oxide, followed by reaction with PCl 3 to give the final product. The continuous flow methodology was used to minimise accumulation of the highly energetic and potentially explosive nitration product to enable the safe scale-up of 4-nitropyridine with no 2-nitropyridine by-product. By employing continuous extraction in the nitration step and applying the optimised conditions, a throughput of 0.716 kg 4-nitropyridine product per day from pyridine N-oxide with 83% yield and high selectivity in a continuous flow system was achieved.
机译:在两个步骤中,由吡啶N-氧化物成功地制备了4-硝基硝基吡啶(医药产品的关键中间体)。用HNO 3和H 2 SO 4硝化吡啶N-氧化物,得到4-硝基吡啶N-氧化物,然后与PCl 3反应,得到最终产物。连续流方法用于最大程度地减少高能硝化和潜在爆炸性硝化产物的积累,以实现4-硝基吡啶的安全放大生产,而没有2-硝基吡啶副产物。通过在硝化步骤中采用连续萃取并应用优化的条件,在连续流系统中,每天从吡啶N-氧化物获得0.716 kg 4-硝基吡啶产物的通量,产率为83%,选择性高。

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