ChemicalBook--->CAS DataBase List--->958030-46-1

958030-46-1

958030-46-1 Structure

958030-46-1 Structure
IdentificationBack Directory
[Name]

Boronic acid, B-(2-formyl-3-methoxyphenyl)-
[CAS]

958030-46-1
[Synonyms]

(2-Formyl-3-methoxyphenyl)boronic acid
(3-methoxy-2-formyl-phenyl)boronic acid
Boronic acid, B-(2-formyl-3-methoxyphenyl)-
[Molecular Formula]

C8H9BO4
[MDL Number]

MFCD01319042
[MOL File]

958030-46-1.mol
[Molecular Weight]

179.97
Chemical PropertiesBack Directory
[Boiling point ]

408.3±55.0 °C(Predicted)
[density ]

1.25±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

7.75±0.53(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[HS Code ]

2931900090
Spectrum DetailBack Directory
[Spectrum Detail]

Boronic acid, B-(2-formyl-3-methoxyphenyl)-(958030-46-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Triisopropyl borate

5419-55-6

Boronic acid, B-(2-formyl-3-methoxyphenyl)-

958030-46-1

General procedure for the synthesis of 3-methoxy-2-formylphenylboronic acid from triisopropyl borate: tert-butyllithium solution (9.0 mL, 1.7 M in pentane) was added dropwise to a stirring solution of 2-(2-methoxyphenyl)-1,3-dimethylimidazolidinium (2.0 g, 9.8 mmol) in tetrahydrofuran (5 mL) under nitrogen protection, and the reaction temperature was maintained at -10 °C, followed by continued stirring at 0-5 °C for 2 hours. Upon completion of the reaction, the mixture was cooled to -50 °C and triisopropyl borate (3.5 mL, 15 mmol) was slowly added. The reaction solution was gradually warmed to 0 °C over 3 hours. 2N hydrochloric acid (120 mL) was added at 0 °C and stirred for 30 min. The reaction mixture was returned to room temperature and diluted with ethyl acetate. The organic phase was washed sequentially with 1N hydrochloric acid (2×) and saturated saline, dried over anhydrous sodium sulfate and concentrated to give a yellow crude product. The crude product was purified by reversed-phase high-performance liquid chromatography, and after removal of the solvent, 1.3 g of 3-methoxy-2-formylphenylboronic acid in the form of a light yellow solid was obtained in 75% yield.ESI-MS m/e 177 (MH+).

[References]

[1] Patent: US2007/270406, 2007, A1. Location in patent: Page/Page column 31
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