Basic information Safety Supplier Related

4-BUTOXY-3-FLUOROPHENYLBORONIC ACID

Basic information Safety Supplier Related

4-BUTOXY-3-FLUOROPHENYLBORONIC ACID Basic information

Product Name:
4-BUTOXY-3-FLUOROPHENYLBORONIC ACID
Synonyms:
  • Boronic acid, B-(4-butoxy-3-fluorophenyl)-
CAS:
156487-13-7
MF:
C10H14BFO3
MW:
212.03
Product Categories:
  • Aryl
  • Boronic Acids
  • Boronic Acids and Derivatives
  • blocks
  • BoronicAcids
Mol File:
156487-13-7.mol
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4-BUTOXY-3-FLUOROPHENYLBORONIC ACID Chemical Properties

Melting point:
91-96 °C(lit.)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
Appearance
White to off-white Solid
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Safety Information

WGK Germany 
3
HS Code 
2931900090
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4-BUTOXY-3-FLUOROPHENYLBORONIC ACID Usage And Synthesis

Synthesis

121-43-7

54509-63-6

156487-13-7

4-Butoxy-3-fluorophenylboronic acid (T-9) was synthesized as follows: 4-bromo-1-butoxy-2-fluorobenzene (T-8) (97.5 g) prepared in the previous step was dissolved in dry tetrahydrofuran (THF) (500 ml) and the solution was cooled to -70 °C. Under nitrogen protection, n-butyllithium (n-BuLi) (241 ml) was slowly added dropwise with continuous stirring for 2 h at a maintained temperature of -70°C. Subsequently, a dry THF solution of trimethyl borate (62.4 g) was slowly added dropwise to the reaction system at the same temperature. The reaction mixture was gradually warmed to room temperature and stirring was continued for 16 hours. After completion of the reaction, 2N hydrochloric acid (HCl) (200 ml) was added to the reaction mixture for acidification. The mixture was extracted with toluene and after separating the organic layer, it was washed sequentially with water and saturated saline and finally dried with anhydrous magnesium sulfate. The organic phase was concentrated under reduced pressure to give a light brown solid product. Purification by recrystallization (solvent ratio: heptane/toluene=4:1, v/v) gave the target compound 4-butoxy-3-fluorophenylboronic acid (T-9) as a colorless powder (54.8 g) in 66% yield.

References

[1] Patent: EP2399896, 2011, A1. Location in patent: Page/Page column 38

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