Dibenzofuran-4-boronic acid Chemical Properties

Melting point:

286-291 °C (lit.)

Boiling point:

438.5±37.0 °C(Predicted)

Density 

1.34±0.1 g/cm3(Predicted)

storage temp. 

Keep in dark place,Sealed in dry,Room Temperature

pka

8.04±0.30(Predicted)

form 

powder

color 

white to off-white

BRN 

1645426

InChIKey

ZXHUJRZYLRVVNP-UHFFFAOYSA-N

CAS DataBase Reference

100124-06-9(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

37/39-26-24/25

WGK Germany 

3

TSCA 

No

HazardClass 

IRRITANT

HS Code 

29321900

MSDS

• Language:English Provider:ACROS
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

Dibenzofuran-4-boronic acid Usage And Synthesis

Description

Dibenzofuran-4-boronic acid (DBFBA) is a boronic acid that has been used as a cross-coupling agent in the Suzuki coupling reaction. It has been shown to have low efficiency, but advances in this area have been made through the use of methanol extraction and photophysical properties. DBFBA is often coupled with imidazole derivatives to form anti-inflammatory compounds. The bond cleavage and hydrogen bonding properties of DBFBA make it a good target for drug synthesis.

Chemical Properties

off-white to beige powder

Uses

Dibenzofuran-4-boronic acid is a water-soluble boronic acid, and the boronic acid molecule is a very useful functional group for the preparation of glycosensors. Water-soluble boronic acids that change their fluorescence properties upon binding to sugars are particularly useful as reporter units for carbohydrate fluorescence sensors. Dibenzofuran-4-boronic acid displays distinctive fluorescence changes at three wavelengths when bound to sugars under near-physiological conditions^[1].

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 80%).

References

[1] JUNFENG WANG Binghe W Shan Jin. A new boronic acid fluorescent reporter that changes emission intensities at three wavelengths upon sugar binding[J]. Tetrahedron Letters, 2005. DOI:10.1016/j.tetlet.2005.08.053.

Dibenzofuran-4-boronic acid(100124-06-9)Related Product Information

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• 4-(DIMETHOXYMETHYL)-2-METHYLPYRIMIDINE
• 4-Chlorobiphenyl
• 4-DIBENZOTHIOPHENEBORONIC ACID
• 4-Bromodiphenylamine
• 4-BROMO-P-TERPHENYL
• 4-Bromophenoxybenzene
• DIBENZOFURAN-4-CARBOXALDEHYDE 97
• Dibenzo[b,d]furan-2-ylboronic acid
• dibenzo[b,d]furan-3-ylboronic acid
• DIBENZOFURAN-2-CARBOXALDEHYDE
• 2-Fluoro-3-pyridylboronic acid
• 2-Chloro-3-pyridylboronic acid
• 5-Chloro-2-fluoropyridin-3-ylboronic acid
• Phenylboronic acid
• Methylboronic acid
• Dibenzofuran
• DIBENZOFURAN-4-BORONIC ACID