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408502-23-8

408502-23-8 Structure

408502-23-8 Structure
IdentificationBack Directory
[Name]

2-METHOXYLYPYRIDINE-4-BORONIC ACID PINACOLATE
[CAS]

408502-23-8
[Synonyms]

2-methoxypyridine-4-boronic acid pinacolate
2-Methoxylypyrinine-4-boronic acid pinacolate
2-Methoxy-4-pyridylboronic Acid Pinacol Ester
2-METHOXYLYPYRIDINE-4-BORONIC ACID PINACOLATE
2-METHOXYPYRIDINE-4-BORONIC ACID PINACOL ESTER
2-Methoxypyridine-4-boronic acid, pinacol ester 97%
2-Methoxy-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
2-(2-Methoxy-4-pyridyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-METHOXYLYPYRIDINE-4-BORONIC ACID PINACOLATE ISO 9001:2015 REACH
2-Methoxy-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridine
Pyridine, 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C12H18BNO3
[MDL Number]

MFCD07368867
[MOL File]

408502-23-8.mol
[Molecular Weight]

235.09
Chemical PropertiesBack Directory
[Melting point ]

36 °C
[Boiling point ]

329.1±27.0 °C(Predicted)
[density ]

1.06±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[solubility ]

soluble in Methanol
[form ]

powder to lump
[pka]

2.56±0.10(Predicted)
[color ]

White to Almost white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2-METHOXYLYPYRIDINE-4-BORONIC ACID PINACOLATE(408502-23-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-IODO-2-METHOXYPYRIDINE

98197-72-9

Bis(pinacolato)diboron

73183-34-3

2-METHOXYLYPYRIDINE-4-BORONIC ACID PINACOLATE

408502-23-8

A mixture of 4-iodo-2-methoxypyridine (0.099 g, 0.42 mmol), pinacol ester of bis(boronic acid) (0.12 g, 0.47 mmol), and potassium acetate (0.13 g, 1.31 mmol) was added to a microwave reactor containing dimethylformamide (1 mL) protected by nitrogen and nitrogen was bubbled for 5 min. Subsequently, [1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloride complex with dichloromethane (1:1) (0.017 g, 0.02 mmol) was added, and the reactor was sealed, and microwave irradiation was carried out for 4 hr at 80 °C. After completion of the reaction, the mixture was diluted with ethyl acetate and filtered through diatomaceous earth. The filtrate was washed sequentially with saturated aqueous sodium bicarbonate, water and brine, dried over anhydrous magnesium sulfate and concentrated to give 2-methoxypyridine-4-boronic acid pinacol ester (0.28 g, 82% yield) as a brown oil, which can be used directly in the next step of the reaction.LRMS (m/z): 236 (M + 1).

[References]

[1] Patent: WO2011/76419, 2011, A1. Location in patent: Page/Page column 131
[2] Patent: EP2338888, 2011, A1. Location in patent: Paragraph 0213; 0214
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