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848243-23-2

848243-23-2 Structure

848243-23-2 Structure
IdentificationBack Directory
[Name]

2-ETHOXY-3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDINE
[CAS]

848243-23-2
[Synonyms]

2-ETHOXYPYRIDINE-3-BORONIC ACID, PINACOL ESTER
2-ethoxy-3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridine
2-ETHOXY-3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDINE
Pyridine, 2-ethoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
2-ethoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine(SALTDATA: FREE)
[Molecular Formula]

C13H20BNO3
[MDL Number]

MFCD07366721
[MOL File]

848243-23-2.mol
[Molecular Weight]

249.11
Chemical PropertiesBack Directory
[Boiling point ]

344.7±27.0 °C(Predicted)
[density ]

1.05±0.1 g/cm3(Predicted)
[storage temp. ]

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

solid
[pka]

4.03±0.24(Predicted)
[Appearance]

Colorless to light yellow Liquid
[CAS DataBase Reference]

848243-23-2
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319
[Precautionary statements ]

P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2-ETHOXY-3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDINE(848243-23-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-BROMO-2-ETHOXYPYRIDINE

57883-25-7

Bis(pinacolato)diboron

73183-34-3

2-ETHOXY-3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDINE

848243-23-2

A suspension was prepared in DMSO (100 mL) with 3-bromo-2-ethoxypyridine (28.69 g, 142.0 mmol), bis(pinacolato)diboron (43.3 g, 170.5 mmol) and potassium acetate (41.8 g, 425.9 mmol). The suspension was degassed with nitrogen and [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (5.8 g, 7.93 mmol) was added. The reaction mixture was stirred at 95 °C for 6 hours. After completion of the reaction, the reaction mixture was filtered through an Arbocel pad and washed with ethyl acetate (500 mL). The filtrate was concentrated under vacuum and the crude product was purified by silica gel column chromatography using a 50% cyclohexane solution of ethyl acetate as eluent to afford 2-ethoxypyridine-3-boronic acid pinacol ester as a red oil (34.4 g, 74% yield).1H NMR (400 MHz, CDCl3) data were as follows: δ 1.35 (s, 12H), 1.39 (m, 3H). 4.37 (m, 2H), 6.81 (m, 1H), 7.89 (m, 1H), 8.19 (m, 1H).Results of LCMS analysis: retention time (Rt) = 3.27 min, mass spectrum (MS) m/z 250 [MH]+.

[References]

[1] Patent: WO2013/93688, 2013, A1. Location in patent: Page/Page column 44-45
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