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ChemicalBook >  Product Catalog >  Inorganic chemistry >  Inorganic salts >  Borides, borates and borate >  METHYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE

METHYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE

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METHYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE Basic information

Product Name:
METHYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE
Synonyms:
  • 3-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
  • 2-METHOXYCARBONYLPHENYLBORONIC ACID, PINACOL ESTER
  • METHYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE
  • 2-(Methoxycarbonyl)benzeneboronic acid, pinacol ester
  • N-Methyltetrahydrothiophene-3-amine-1,1-dioxidehydrochloride
  • Methyl 2-(4
  • Methyl 2-((4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)Methyl)benzoate
  • Benzoic acid, 2-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-, Methyl ester
CAS:
653589-95-8
MF:
C14H19BO4
MW:
262.11
EINECS:
600-611-8
Product Categories:
  • Acids and Derivatives
  • Boron, Nitrile, Thio,& TM-Cpds
  • blocks
  • BoronicAcids
Mol File:
653589-95-8.mol
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METHYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE Chemical Properties

Melting point:
49-51°C
Boiling point:
363.7±25.0 °C(Predicted)
Density 
1.08±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to lump to clear liquid
color 
White or Colorless to Almost white or Almost colorless
CAS DataBase Reference
653589-95-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
WGK Germany 
3
HS Code 
2931900090
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METHYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE Usage And Synthesis

Chemical Properties

White powder

Synthesis

610-94-6

73183-34-3

653589-95-8

Methyl o-bromobenzoate (2.15 g, 10 mmol), bis(pinacolato)diboron (3.05 g, 12 mmol), potassium acetate (3.92 g, 40 mmol), and [1,1'-bis(diphenylphosphino)ferrocene]palladium dichloride (0.49 g, 0.5 mmol) were sequentially added to 150 mL of dioxane under nitrogen atmosphere. The reaction mixture was heated to 85 °C and the reaction was stirred at this temperature for 12 hours. Upon completion of the reaction, the solvent dioxane was removed by distillation under reduced pressure. The residue was extracted with dichloromethane and the combined organic phases were washed three times with saturated aqueous sodium chloride solution. The organic phases were dried over anhydrous sodium sulfate and the dichloromethane was removed by distillation under reduced pressure to give the crude product. The crude product was purified by column chromatography, and the eluent was a mixed solvent of petroleum ether and dichloromethane (3:1, v/v) to give 2-methoxycarbonylphenylboronic acid pinacol ester as a white solid (1.25 g, 86% yield). The structure of the product was confirmed by 1H NMR, 13C NMR, mass spectrometry (MS) and elemental analysis.

References

[1] Patent: CN108424344, 2018, A. Location in patent: Paragraph 0062; 0063; 0064; 0074
[2] Patent: KR2015/111106, 2015, A. Location in patent: Paragraph 0383-0386
[3] Patent: KR2016/2328, 2016, A. Location in patent: Paragraph 0589-0591
[4] Patent: KR2017/139895, 2017, A. Location in patent: Paragraph 0395; 0414-0419
[5] Green Chemistry, 2012, vol. 14, # 3, p. 661 - 667

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