化学
催化作用
硝基
填充床
碳纤维
镍
选择性
硅胶
氢
氮气
无机化学
有机化学
色谱法
复合数
材料科学
复合材料
烷基
作者
Lei Cao,Syed Asad Abbas,Seo Hyeon Jeong,Dongho Seo,Ki Min Nam,Jin Kyoon Park
标识
DOI:10.1002/adsc.202300357
摘要
Abstract Selective reduction of nitro‐containing arenes and heteroarenes was achieved in 5 minutes at room temperature utilizing inexpensive NaBH 4 as a hydrogen source and a newly developed Ni@N−C catalyst, obtained via a simple carbon coating process without the need for an external carbon source. A wide variety of nitro derivatives, including pharmaceutical molecules, was successfully reduced to the corresponding amines in yields ranging from 45% to 99% using the Ni@N−C catalyst under general batch conditions. The reactivity and selectivity of the nitro reduction were further enhanced by a continuous flow reaction system, especially when a newly designed Y‐type column was used, and the Osimertinib intermediate was produced on gram scale after 24 hours without any nickel metal contamination or silica gel chromatography purification.
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