Literature DB >> 24554581

Continuous-flow synthesis of functionalized phenols by aerobic oxidation of Grignard reagents.

Zhi He1, Timothy F Jamison.   

Abstract

Phenols are important compounds in chemical industry. An economical and green approach to phenol preparation by the direct oxidation of aryl Grignard reagents using compressed air in continuous gas-liquid segmented flow systems is described. The process tolerates a broad range of functional groups, including oxidation-sensitive functionalities such as alkenes, amines, and thioethers. By integrating a benzyne-mediated in-line generation of arylmagnesium intermediates with the aerobic oxidation, a facile three-step, one-flow process, capable of preparing 2-functionalized phenols in a modular fashion, is established.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Grignard reagent; chemoselectivity; flow chemistry; oxidation; phenol

Mesh:

Substances:

Year:  2014        PMID: 24554581     DOI: 10.1002/anie.201310572

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  9 in total

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Review 4.  Continuous Flow Aerobic Alcohol Oxidation Reactions Using a Heterogeneous Ru(OH) x /Al2O3 Catalyst.

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8.  Continuous flow synthesis of diaryl ketones by coupling of aryl Grignard reagents with acyl chlorides under mild conditions in the ecofriendly solvent 2-methyltetrahydrofuran.

Authors:  Chuan-Tao Zhang; Rui Zhu; Zheng Wang; Bing Ma; Adrian Zajac; Marcin Smiglak; Chun-Nian Xia; Steven L Castle; Wen-Long Wang
Journal:  RSC Adv       Date:  2019-01-17       Impact factor: 3.361

9.  Preparation of 3-hydroxyquinolines from direct oxidation of dihydroquinolinium salts.

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  9 in total

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