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CAS 220210-56-0

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3-(tert-Butoxycarbonyl)phenylboronic acid

Description:
3-(tert-Butoxycarbonyl)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a tert-butoxycarbonyl (Boc) group. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as dichloromethane and methanol, but has limited solubility in water. The presence of the boronic acid group allows for participation in various chemical reactions, including Suzuki coupling, which is valuable in organic synthesis for forming carbon-carbon bonds. The tert-butoxycarbonyl group serves as a protective group for amines, making this compound useful in the synthesis of more complex molecules. Additionally, the compound's reactivity can be influenced by the electronic effects of the phenyl ring and the steric hindrance introduced by the tert-butyl group. Overall, 3-(tert-Butoxycarbonyl)phenylboronic acid is a versatile intermediate in organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C11H15BO4
InChI:InChI=1/C11H15BO4/c1-11(2,3)16-10(13)8-5-4-6-9(7-8)12(14)15/h4-7,14-15H,1-3H3
InChI key:InChIKey=HVJDVHCPCSZDSR-UHFFFAOYSA-N
SMILES:CC(C)(C)OC(=O)c1cccc(c1)B(O)O
Synonyms:
  • (3-(tert-Butoxycarbonyl)phenyl)boronic acid
  • (3-[[(1,1-Dimethylethyl)oxy]carbonyl]phenyl)boronic acid
  • 1-(1,1-Dimethylethyl) 3-boronobenzoate
  • 3-(tert-Butoxycarbonyl)benzeneboronic acid
  • 3-tert-Butoxycarbonylphenylboronic acid
  • 3-tert-Butoxycarbonylphenylboronicacid
  • Benzoic acid, 3-borono-, 1-(1,1-dimethylethyl) ester
  • [3-[(2-Methylpropan-2-yl)oxycarbonyl]phenyl]boronic acid
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