Revisiting aromatic diazotization and aryl diazonium salts in continuous flow: highlighted research during 2001–2021

文献信息

发布日期 2022-02-28
DOI 10.1039/D2RE00001F
影响因子 4.239
作者

Jianli Chen, Xiaoxuan Xie, Jiming Liu, Zhiqun Yu, Weike Su


查看原文

摘要

Aryl diazonium salts play an important role in chemical transformations; however their explosive nature limits their applications in batch. Continuous flow technology allows safer operation for diazotization and application of aryl diazonium salts. Moreover, the other characteristics of continuous flow, such as laminar flow, residence time control, flow reactors with a larger surface area-to-volume ratio, the flexibility of equipment, etc., have significantly improved the reaction efficiency and industrialization potential of diazotization and aryl diazonium salts in various types of chemical transformations. However, the transformation from batch to continuous flow is still accompanied by new challenges (e.g., solid management, automation, and process analytical technology). Therefore, the application of aryl diazonium salts in continuous flow systems is closely related to the upgrade of continuous flow technology. In this article, an overview of aromatic diazotization and applications of aryl diazonium salts in continuous flow systems was described in detail.

相关文献

Thermally stable ordered mesoporous CeO2/TiO2 visible-light photocatalysts

Guisheng Li, Dieqing Zhang, Jimmy C. Yu

2009-02-25 Paper

DOI: 10.1039/B819167K

Structural diversity of dimers of the Alzheimer amyloid-β(25–35) peptide and polymorphism of the resulting fibrils

Guanghong Wei, Andrew I. Jewett, Joan-Emma Shea

2010-03-11 Paper

DOI: 10.1039/C000755M

Back cover

Front/Back Matter

DOI: 10.1039/C004145A

Nature of proton dynamics in a polymer electrolyte membrane, nafion: a first-principles molecular dynamics study

Yoong-Kee Choe, Eiji Tsuchida, Tamio Ikeshoji, Shunsuke Yamakawa, Shi-aki Hyodo

2009-03-14 Paper

DOI: 10.1039/B819535H

Thymine relaxation after UV irradiation: the role of tautomerization and πσ* states

Jesús González-Vázquez, Leticia González, Elena Samoylova, Thomas Schultz

2009-03-13 Paper

DOI: 10.1039/B815602F

Contents

Front/Back Matter

DOI: 10.1039/C004645K

Back cover

Front/Back Matter

DOI: 10.1039/C004808A

您可能还喜欢

化合物问答

如何处理含有顺-二(2,2'-联吡啶)二氯化钌(II)二水合物(CAS号:67776-38-9)的废料?

处理含有该化合物的废料时,应先收集并分类,然后根据其危险特性选择合适的处理方法。推荐采用焚烧或由专业机构进行安全处理,以确保符合环保法规的要求。处理过程中应佩戴...

67776-38-93-{[(2R,3R,4S,5R,6R)...
化合物问答

4-amino-2-bromo-3-iodopyridine(CAS号:1300750-77-9)的市场或研究趋势如何?

4-氨基-2-溴-3-碘吡啶主要应用于药物合成和研究领域,尤其是在抗病毒和抗癌药物的研发中。随着新型药物的需求增加,该化合物的研究趋势较好。市场方面,由于其特殊...

1300750-77-92-bromo-3-iodopyridi...
化合物问答

4-乙酰基氨基-2-氨基-苯甲酸(CAS号:43134-76-5)的市场或研究趋势如何?

当前,4-乙酰基氨基-2-氨基-苯甲酸(CAS号:43134-76-5)在医药和化工领域有一定的应用。随着药物研发的进展,该化合物在新型药物设计中的应用可能增加...

43134-76-54-Acetamido-2-aminob...
化合物问答

庚a氟-1-(1-碘-1,2,2,2-四氟乙氧基)丙烷(CAS号:107432-46-2)的市场或研究趋势如何?

该化合物目前主要用于特定的工业应用,如氟聚合物的合成。市场趋势显示,由于其独特的结构和性能,未来可能在新型氟材料和特种化学品领域有更多的应用。研究趋势方面,主要...

107432-46-21,1,1,2,2,3,3-Heptaf...
化合物问答

在合成中是否有Propargyl-PEG13-bromide(CAS号:2055105-25-2)的替代品?

可以考虑使用1,3-丁二烯-1-炔-3-基-聚乙二醇-13-溴化物作为Propargyl-PEG13-bromide的替代品,因为两者在结构上相似,均可用于合成...

2055105-25-2Propargyl-peg13-brom...
化合物问答

2-氨基-6-甲氧基嘌呤(CAS号:20535-83-5)安全吗?

2-氨基-6-甲氧基嘌呤在正常使用条件下相对安全,但在操作时仍需注意防护措施,如佩戴手套和护目镜,避免吸入或接触皮肤和眼睛。

20535-83-56-Methoxy-7H-purin-2...
化合物问答

2-甲基-3-溴苯乙酸乙酯(CAS号:1261862-72-9)适用哪些法规指南?

该化合物根据其化学性质和潜在危害,可能适用于GHS(全球化学品统一分类和标签制度)的分类标准。具体分类需依据其毒性和燃烧危险性进行评估。此外,欧洲化学品管理局(...

1261862-72-9Ethyl (3-bromo-2-met...
化合物问答

4,4-二甲基吡咯烷-3-羧酸盐酸盐(CAS号:1351343-41-3)应用于哪些行业?

4,4-二甲基吡咯烷-3-羧酸盐酸盐在医药、聚合物和传感器领域有应用。在医药领域,它可以作为某些药物的中间体;在聚合物领域,它可用作某些聚合物的稳定剂;在传感器...

1351343-41-34,4-Dimethyl-3-pyrro...
化合物问答

处理5-Hydroxy-7-methoxy-2-(4-methoxyphenyl)-4-oxo-4H-chromen-6-yl 2-O-beta-D-xylopyranosyl-beta-D-glucopyranoside(CAS号:149998-39-0)时应注意哪些实验室安全事项?

处理该化合物时应注意使用个人防护装备(如手套、护目镜和实验服),在通风橱中操作。避免直接接触皮肤和吸入,泄漏时应立即清理并使用适当的吸收材料。参考安全数据表(S...

149998-39-05-Hydroxy-7-methoxy-...
化合物问答

7-甲基-1,2,3,4-四氢-吖啶-9-甲酸(CAS号:345621-27-4)的市场或研究趋势如何?

该化合物在医药研究中具有潜在应用价值,特别是在抗癌药物研发方面。随着研究的深入,对其合成方法的优化和生物活性的进一步探索将成为研究热点。

345621-27-47-Methyl-1,2,3,4-tet...

来源期刊

Reaction Chemistry & Engineering

Reaction Chemistry & Engineering
CiteScore: 0
自引率: 8.8%
年发文量: 284

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.

推荐供应商

免责声明
本页面提供的学术期刊信息仅供参考和研究使用。我们与任何期刊出版商均无关联,也不处理投稿事宜。如有投稿相关咨询,请直接联系相关期刊出版商。
如发现页面信息有误,请发送邮件至 support@chemtradehub.com 联系我们。我们将及时核实并处理您的问题。