Basic information Safety Supplier Related

2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE

Basic information Safety Supplier Related

2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE Basic information

Product Name:
2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE
Synonyms:
  • 2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE
  • 3,5-DIMETHOXYPHENYLBORONIC ACID, PINACOL ESTER
  • 3,5-Dimethoxyphenylboronic acid pinacol ester 97%
  • 1,3,2-Dioxaborolane, 2-(3,5-dimethoxyphenyl)-4,4,5,5-tetramethyl-
  • 1,3-Dimethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
  • 3,5-Dimethoxybenzeneboronic acid pinacol ester
CAS:
365564-07-4
MF:
C14H21BO4
MW:
264.13
Mol File:
365564-07-4.mol
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2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE Chemical Properties

Melting point:
90-94 °C(lit.)
Boiling point:
374.5±32.0 °C(Predicted)
Density 
1.05
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Almost white
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
2931900090

MSDS

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2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE Usage And Synthesis

Synthesis

73183-34-3

151-10-0

365564-07-4

Under nitrogen protection, 1,3-dimethoxybenzene (69.1 mg, 0.5 mmol), pinacol ester of bisboronic acid (126.9 mg, 0.5 mmol), methoxy-1,5-cyclooctadienyl iridium dimer (3.4 mg, 0.005 mmol, 1 mol%), and borane pyridine ligand (4.0 mg, 0.01 mmol, 2 mol%), followed by the addition of cyclopentyl methyl ether (1 mL to give a 1,3-dimethoxybenzene concentration of 0.5 mol/L). The reaction mixture was stirred at 100°C for 16 hours. After completion of the reaction, the solvent cyclopentyl methyl ether was removed by rotary evaporation (20-40°C). The crude product was purified by column chromatography (using 200-300 mesh silica gel with a silica gel to sample mass ratio of 50-100:1 and an eluent that was a mixture of petroleum ether and ethyl acetate at a volume ratio of 20-50:1) to give 3,5-dimethoxyphenylboronic acid pinacol ester as a colorless solid (125 mg, 99% yield).

References

[1] Patent: CN104725409, 2016, B. Location in patent: Paragraph 0036; 0037; 0040
[2] Journal of the American Chemical Society, 2015, vol. 137, # 25, p. 8058 - 8061
[3] Research on Chemical Intermediates, 2013, vol. 39, # 4, p. 1917 - 1926
[4] Journal of the American Chemical Society, 2015, vol. 137, # 15, p. 5193 - 5198
[5] Chemistry - A European Journal, 2017, vol. 23, # 26, p. 6282 - 6285

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