Home Chemistry Organic Building Blocks Chlorides (3-Chlorophenyl)Boronic Acid
These compounds have the same murcko framework: benzene,and at least 2 kinds of functional groups( —Cl,—B(OH)2).
Sandmeyer Reaction: Chlorobenzene can be converted to other aryl halides through the Sandmeyer reaction, involving replacement of the chlorine atom with other halogens.
Formation of 【esters|https://www.ambeed.com/esters.html】 and 【Amides|https://www.ambeed.com/amides.html】: Phenylboronic acid can react with 【alcohols|https://www.ambeed.com/alcohols.html】 or 【amines|https://www.ambeed.com/amines.html】 to form 【esters|https://www.ambeed.com/esters.html】 and 【amides|https://www.ambeed.com/amides.html】, respectively, under appropriate conditions.
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(3-Chloro-4-(chlorocarbonyl)phenyl)boronic acid
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6-Bromo-3-chloro-2-fluorophenylboronic acid
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(3-Chloro-4-methanesulfonylphenyl)boronic acid
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(3-Chloro-4-(methylthio)phenyl)boronic acid
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(3,5-Dichloro-4-methoxyphenyl)boronic acid
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(3-Chloro-4-ethoxy-5-fluorophenyl)boronic acid
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(5-Chloro-2,4-difluorophenyl)boronic acid
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(3-Chloro-4-(methoxycarbonyl)phenyl)boronic acid
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(3-Chloro-4-(hydroxymethyl)phenyl)boronic acid
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(2,3-Dichloro-6-fluorophenyl)boronic acid
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(3-Chloro-2,4-difluorophenyl)boronic acid
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