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365564-07-4

365564-07-4 Structure

365564-07-4 Structure
IdentificationBack 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 PropertiesBack 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
[InChI]

1S/C14H21BO4/c1-13(2)14(3,4)19-15(18-13)10-7-11(16-5)9-12(8-10)17-6/h7-9H,1-6H3
[InChIKey]

CZYHRTIJLUONKY-UHFFFAOYSA-N
[SMILES]

COc1cc(OC)cc(c1)B2OC(C)(C)C(C)(C)O2
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[HS Code ]

2931900090
[Storage Class]

13 - Non Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE(365564-07-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

Bis(pinacolato)diboron

73183-34-3

1,3-Dimethoxybenzene

151-10-0

2-(3,5-DIMETHOXY)-PHENYL-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROLANE

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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