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BENZOFURAN-5-BORONIC ACID

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BENZOFURAN-5-BORONIC ACID Basic information

Product Name:
BENZOFURAN-5-BORONIC ACID
Synonyms:
  • 5-Benzofuranylboronic acid
  • Boronic acid, B-5-benzofuranyl-
  • 1-Benzofuran-5-boronic acid, 5-Borono-1-benzofuran
  • ENZOFURAN-5-BORONIC ACID
  • BENZOFURAN-5-BORONIC ACID
  • AKOS BRN-0183
  • Akos ba-183
  • benzofuran-5-yl-5-boronic acid
CAS:
331834-13-0
MF:
C8H7BO3
MW:
161.95
Mol File:
331834-13-0.mol
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BENZOFURAN-5-BORONIC ACID Chemical Properties

Boiling point:
340.4±34.0 °C(Predicted)
Density 
1.31±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,2-8°C
form 
solid
pka
8.25±0.30(Predicted)
color 
White to off-white
InChI
InChI=1S/C8H7BO3/c10-9(11)7-1-2-8-6(5-7)3-4-12-8/h1-5,10-11H
InChIKey
WYXQQAYIAJRORT-UHFFFAOYSA-N
SMILES
B(C1=CC=C2OC=CC2=C1)(O)O
CAS DataBase Reference
331834-13-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C
Hazard Note 
Corrosive
HS Code 
2932990090
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BENZOFURAN-5-BORONIC ACID Usage And Synthesis

Synthesis

23145-07-5

121-43-7

331834-13-0

The general procedure for the synthesis of benzo[b]furan-5-boronic acid from 5-bromobenzo[b]furan and trimethyl borate is as follows: 1. a hexane solution of n-butyllithium (1.5 M; 3.72 ml, 5.6 mmol) was slowly added dropwise to a solution of tetrahydrofuran (10 ml) of 5-bromobenzo[b]furan (1.0 g, 5.0 mmol) under argon protection, keeping the reaction temperature at -60°C. 2. stirring was continued at the same temperature for 30 min. 3. trimethyl borate (0.69 ml, 6.0 mmol) was added to the reaction system, followed by slow warming of the reaction mixture to room temperature over a period of 4 hours. 4. Water (5 ml) was added to the reaction mixture and cooled to 5 °C, followed by distillation under reduced pressure to remove the tetrahydrofuran. 5. The pH was adjusted to 1 by adding 1N hydrochloric acid to the residue and then extracted with ethyl acetate. 6. The organic layer was washed with brine, dried and the solvent was removed by distillation. 7. The residue was ground with hexane/ether mixture, filtered and dried to give benzo[b]furan-5-boronic acid (551 mg) in light brown solid form.

References

[1] Patent: EP2959918, 2015, A1. Location in patent: Paragraph 0089

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