2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE
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
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
Safety Information
- Safety Statements
- 22-24/25
- WGK Germany
- 3
- HS Code
- 2931900090
MSDS
- Language:English Provider:SigmaAldrich
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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