Facile one-pot reduction of β-nitrostyrenes to phenethylamines using sodium borohydride and copper(II) chloride.

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC Beilstein Journal of Organic Chemistry Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI:10.3762/bjoc.21.4
Laura D'Andrea, Simon Jademyr
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引用次数: 0

Abstract

Phenethylamines and phenylisopropylamines of scientific relevance can be prepared with a NaBH4/CuCl2 system in 10 to 30 minutes via reduction of substituted β-nitrostyrenes. This one-pot procedure allows the quick isolation of substituted β-nitrostyrene scaffolds with 62-83% yield under mild conditions, without the need for special precautions, inert atmosphere, and time-consuming purification techniques.

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用硼氢化钠和氯化铜一锅简易还原β-硝基苯乙烯为苯乙胺。
在NaBH4/CuCl2体系中,通过取代β-硝基苯乙烯的还原反应,可以在10 ~ 30分钟内制备出具有科学意义的苯乙胺和苯异丙胺。此一锅程序允许在温和条件下快速分离取代β-硝基苯乙烯支架,产率为62-83%,无需特殊预防措施,惰性气氛和耗时的净化技术。
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来源期刊
CiteScore
4.90
自引率
3.70%
发文量
167
审稿时长
1.4 months
期刊介绍: The Beilstein Journal of Organic Chemistry is an international, peer-reviewed, Open Access journal. It provides a unique platform for rapid publication without any charges (free for author and reader) – Platinum Open Access. The content is freely accessible 365 days a year to any user worldwide. Articles are available online immediately upon publication and are publicly archived in all major repositories. In addition, it provides a platform for publishing thematic issues (theme-based collections of articles) on topical issues in organic chemistry. The journal publishes high quality research and reviews in all areas of organic chemistry, including organic synthesis, organic reactions, natural product chemistry, structural investigations, supramolecular chemistry and chemical biology.
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