Identification | Back Directory | [Name]
2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE | [CAS]
365564-07-4 | [Synonyms]
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- 2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE 1,3-Dimethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene | [Molecular Formula]
C14H21BO4 | [MDL Number]
MFCD05865191 | [MOL File]
365564-07-4.mol | [Molecular Weight]
264.13 |
Chemical Properties | Back Directory | [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 |
Hazard Information | Back Directory | [Synthesis]
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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Energy Chemical
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