Home Chemistry Organic Building Blocks Trifluoromethyls (2-(Trifluoromethoxy)Phenyl)Boronic Acid
These compounds have the same murcko framework: benzene,and at least 2 kinds of functional groups( —OCF3,—B(OH)2).
Cross-Coupling Reactions: Trifluoromethoxybenzene can be used as a substrate in various cross-coupling reactions, such as Suzuki-Miyaura coupling, Heck coupling, or Buchwald-Hartwig amination. These reactions can introduce various substituents onto the benzene ring.
Hydroboration: Phenylboronic acid can undergo hydroboration reactions with 【alkenes|https://www.ambeed.com/alkenyls.html】 or 【alkynes|https://www.ambeed.com/alkynyls.html】, leading to the formation of organoboranes. These can subsequently be transformed into various functional groups.
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5-Hydroxy-2-(trifluoromethoxy)phenylboronic acid
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(5-Bromo-2-(trifluoromethoxy)phenyl)boronic acid
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(5-Cyano-2-(trifluoromethoxy)phenyl)boronic acid
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(3-Chloro-2-(trifluoromethoxy)phenyl)boronic acid
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