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dibenzo[b,d]furan-3-ylboronic acid

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dibenzo[b,d]furan-3-ylboronic acid Basic information

Product Name:
dibenzo[b,d]furan-3-ylboronic acid
Synonyms:
  • Boronic acid, 3-dibenzofuranyl-
  • Boronic acid,B-3-dibenzofuranyl-
  • dibenzo[b,d]furan-3-ylboronic acid
  • B-3-dibenzofuranylBoronic acid
  • (3-Dibenzofuranyl)boronic acid
  • Dibenzofuran-3-boronic acid
  • Dibenzofuran-3-ylboronic acid
  • Dibenzo[b,d]furan-3-boronicacid
CAS:
395087-89-5
MF:
C12H9BO3
MW:
212.01
Product Categories:
  • OLED
Mol File:
395087-89-5.mol
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dibenzo[b,d]furan-3-ylboronic acid Chemical Properties

Boiling point:
438.5±37.0 °C(Predicted)
Density 
1.34±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
8.20±0.30(Predicted)
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Safety Information

HS Code 
2931900090
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dibenzo[b,d]furan-3-ylboronic acid Usage And Synthesis

Uses

Dibenzo[b,d]furan-3-ylboronic acid can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development and chemical and pharmaceutical production processes.

Synthesis

In a 300 ml three-necked flask, 7.2 g of 4-bromodibenzofuran was dissolved in ?78° C. anhydrous tetrahydrofuran (THF) under an argon atmosphere. Then, 20 ml of an n-butyl lithium-n-hexane solution (1.6 M, 1.1 eq) was added and stirred for 1 hour. 4.23 ml (1.3 eq) of trimethoxyborane (B(OMe)3) was added and stirred for 2 hours, and the temperature of the reaction system was increased to room temperature. 200 ml of 1 N hydrochloric acid was added into the reactant and stirred for 3 hours. An organic layer was separated, and solvents were distilled off. In the crude product thus obtained, hexane was added. Precipitated product was filtered to obtain 4.94 g of dibenzofuran-4-boronic acid as a white solid (yield 80percent). The product was measured by FAB-MS, and dibenzofuran-4-boronic acid having a molecular weight of 212 was detected.

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