Palladium-Catalyzed Borylation of Aryl Halides in Water Using Poly (Ethylene Glycol)-Based Surfactants

Background: Developing environmentally benign processes, such as organic reactions conducted in water, is desired from the view of sustainable technology. Concerning the palladiumcatalyzed borylation reactions of aryl halides in water, only a few examples have been reported. Objective: This study aimed to develop efficient methods for palladium-catalyzed borylation reactions of aryl halides in water, not only increasing product yields but also extracting products with less organic solvents. Methods: We adopted polymer surfactants, such as diblock copolymers that consist of poly(Nisopropoylacrylamide) and a hydrophilic segment, and a poly(ethylene glycol)-based polymer that consists of poly(ethylene glycol) chain and 4-chloromethylbenzyl moiety. Results: Reactions using these polymers gave the borylation products in significantly higher yields than that in pure water. The efficiency of the extraction process for the products from the reaction mixtures was evaluated, indicating that the polymer micelles enabled separation processes with less organic solvent. Conclusion: Applying polymer surfactants increased the product yields in Pd-catalyzed borylation of aryl halides, and it enabled the extraction of the products from the aqueous reaction mixture more efficiently.

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Publication Details

Journal
Current Organocatalysis
Published
2025-01-10
DOI
https://doi.org/10.2174/0122133372355594241211060459
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
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article

Palladium-Catalyzed Borylation of Aryl Halides in Water Using Poly (Ethylene Glycol)-Based Surfactants

Daisuke Takayama, Zheng Yang, Yuko Takeoka, Masahiro Rikukawa et al.
Current Organocatalysis
Catalytic Cross-Coupling Reactions
article

Palladium-Catalyzed Borylation of Aryl Halides in Water Using Poly (Ethylene Glycol)-Based Surfactants

Daisuke Takayama, Zheng Yang, Yuko Takeoka, Masahiro Rikukawa, Noriyuki Suzuki, K Okajima, Bjarne L. Silkenath
article en

Abstract

Background: Developing environmentally benign processes, such as organic reactions conducted in water, is desired from the view of sustainable technology. Concerning the palladiumcatalyzed borylation reactions of aryl halides in water, only a few examples have been reported. Objective: This study aimed to develop efficient methods for palladium-catalyzed borylation reactions of aryl halides in water, not only increasing product yields but also extracting products with less organic solvents. Methods: We adopted polymer surfactants, such as diblock copolymers that consist of poly(Nisopropoylacrylamide) and a hydrophilic segment, and a poly(ethylene glycol)-based polymer that consists of poly(ethylene glycol) chain and 4-chloromethylbenzyl moiety. Results: Reactions using these polymers gave the borylation products in significantly higher yields than that in pure water. The efficiency of the extraction process for the products from the reaction mixtures was evaluated, indicating that the polymer micelles enabled separation processes with less organic solvent. Conclusion: Applying polymer surfactants increased the product yields in Pd-catalyzed borylation of aryl halides, and it enabled the extraction of the products from the aqueous reaction mixture more efficiently.

Current OrganocatalysisVol. 12(2)
Sophia University (JP)
Responsible consumption and production
Openalex Percentile: Top 100%
Catalytic Cross-Coupling Reactions
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Palladium-Catalyzed Borylation of Aryl Halides in Water Using Poly (Ethylene Glycol)-Based Surfactants — Daisuke Takayama, Zheng Yang, et al. · Current Organocatalysis (2025) | TGRS Research Map | TGRS