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PHENYL-D5-BORONIC ACID

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PHENYL-D5-BORONIC ACID Basic information

Product Name:
PHENYL-D5-BORONIC ACID
Synonyms:
  • PHENYL-D5-BORONIC ACID
  • phenyl-d5-boronicacid98atom%d
  • (Perdeuterophenyl)boronic acid
  • B-(Phenyl-2,3,4,5,6-d5)boronic acid
  • 2,3,4,5,6-Pentadeuteriumbenzeneboronic Acid
  • Boronic acid,B-(phenyl-2,3,4,5,6-d5)-
  • 9-bromo-10-(phenyl-d5)anthracene
  • PHENYL-D5-BORONIC ACID(D, 98%)
CAS:
215527-70-1
MF:
C6H7BO2
MW:
121.93
Product Categories:
  • Boronic Acids
  • blocks
  • BoronicAcids
  • Aryl
  • Boronic Acids
  • Boronic Acids and Derivatives
Mol File:
215527-70-1.mol
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PHENYL-D5-BORONIC ACID Chemical Properties

Melting point:
217-220 °C(lit.)
solubility 
Chloroform (Slightly), DMSO
form 
solid
color 
White
Stability:
Hygroscopic
InChI
InChI=1S/C6H7BO2/c8-7(9)6-4-2-1-3-5-6/h1-5,8-9H
InChIKey
HXITXNWTGFUOAU-RALIUCGRSA-N
SMILES
B(C1C([H])=C([H])C([H])=C([H])C=1[H])(O)O
CAS DataBase Reference
215527-70-1
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
36
WGK Germany 
3
HS Code 
2931900090

MSDS

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PHENYL-D5-BORONIC ACID Usage And Synthesis

Uses

Phenylboronic Acid-d5 is the isotope labelled analog of Phenylboronic Acid; a compound used in the organic synthesis of various pharmaceutical goods.

Synthesis

A dry three-neck flask equipped with a rubber septum, an addition funnel equipped with a rubber septum, and a condenser was charged under nitrogen with magnesium turnings. To the addition funnel was added D5-bromobenzene (6.5 mL, 62 mmol) (Aldrich) dissolved in a 1:1 mixture of THF/toluene (31 mL). Grignard reagent formation was observed after about after about 1 mL of the contents of the addition funnel had been added to the magnesium turnings. The remaining bromobenzene solution was added dropwise over a period of about 1 h. After the addition was complete the reaction mixture was heated at 70° C. for 1 h. The reaction mixture was cooled to room temperature and added via a canulating needled to an addition funnel on a second three-neck flask containing a solution of triethylborate (B(OEt)3) (10.5 mL, 62 mmol) in toluene (10 mL) maintained at 0° C. The solution of the freshly prepared Grignard reagent was then added dropwise to the solution of triethylborate over a period of 1 h. The cooling bath was then removed and the reaction mixture was allowed to stir at room temperature for 15 h. The reaction mixture was quenched with 10% H2SO4 (30 mL) and stirred at room temperature for 1 h. The layers were separated and the organic layer was dried over Na2SO4. After removal of the solvent, addition of hexane precipitated the product as an off-white solid, which was collected by filtration and dried to afford Phenyl-d5-boronic acid. Its yield: 3.50 g, 45%.

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