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653589-95-8

653589-95-8 Structure

653589-95-8 Structure
IdentificationMore
[Name]

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

653589-95-8
[Synonyms]

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
[EINECS(EC#)]

600-611-8
[Molecular Formula]

C14H19BO4
[MDL Number]

MFCD05663866
[Molecular Weight]

262.11
[MOL File]

653589-95-8.mol
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332
[Precautionary statements ]

P260-P280-P312
[Hazard Codes ]

Xi
[WGK Germany ]

3
[HS Code ]

2931900090
Hazard InformationBack Directory
[Chemical Properties]

White powder
[Synthesis]

Methyl 2-bromobenzoate

610-94-6

Bis(pinacolato)diboron

73183-34-3

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

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
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE(653589-95-8)1HNMR
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