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512834 Sigma-Aldrich

3-(Hydroxymethyl)phenylboronic acid

≥95%

Synonym: 3-Hydroxymethylbenzeneboronic acid

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   HGTDLKXUWVKLQX-UHFFFAOYSA-N
assay   ≥95%
mp   95-99 °C (lit.)

Description

Application

Reactant involved in:
• Copper-mediated trifluoromethylation
• Copper-catalyzed transformations from arylboronic acids in water
• Mitsunobu, Suzuki, and amidation reactions with hydroxyphenylamino bromopyrazinecarboxylate

Reactant involved in the synthesis of biologically active molecules including:
• Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors via Suzuki coupling reactions
• HIV protease inhibitors with antiviral activity against drug-resistant viruses
• Pyrrole derivatives for use as PDE4B inhibitors

Packaging

1, 10 g in glass bottle

Other Notes

Contains varying amounts of anhydride

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Arylboronic Acids

We are pleased to present its complete selection of arylboronic acids, the building blocks of the Suzuki coupling experiment. Most arylboronic acids readily undergo dehydration reactions to give a cy...
ChemFiles 2001, 1.1, 5.
Keywords: Building blocks, Coupling reactions, Dehydration reaction, Suzuki coupling

Boronic Acids - ChemFiles 2007

Most boronic acids readily undergo dehydration reactions to give a cyclic (trimer) anhydride. Our selection of boronic acids may contain varying amounts of this cyclic anhydride. Fortunately, the aci...
ChemFiles 2007, 7.7, 3.
Keywords: Coupling reactions, Dehydration reaction, Suzuki coupling

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