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Chemical Structure| 98061-24-6 Chemical Structure| 98061-24-6

Structure of 98061-24-6

Chemical Structure| 98061-24-6

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Product Details of [ 98061-24-6 ]

CAS No. :98061-24-6
Formula : C13H13NO2
M.W : 215.25
SMILES Code : COC1=CC(OC)=C(C2=CC=CC=N2)C=C1
MDL No. :MFCD32065722

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Application In Synthesis of [ 98061-24-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 98061-24-6 ]

[ 98061-24-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 109-04-6 ]
  • [ 133730-34-4 ]
  • [ 98061-24-6 ]
YieldReaction ConditionsOperation in experiment
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In tetrahydrofuran; water;Inert atmosphere; Reflux; In a one-neck round bottom flask, 2-bromopyridine (1.00 g), (2,4-dimethoxyphenyl)boronic acid (1.15 g), and Na2CO3 (2.02 g) (made in accordance with the published procedure in Dalton Trans. 2014, 43 (15), 5667-5679) were stirred in a solution of THF (22.4 mL) and water (9.4 mL) before being degassed by sonicating under vacuum. Pd(PPh3)4 (0.34 g) was added and the solution was heated at reflux overnight under nitrogen. The solvent was removed under reduced pressure and the resulting residue was dissolved in ethyl acetate and washed with water. The aqueous layer was then extracted with ethyl acetate (3×50 mL) and the combined organic extracts were washed with brine and dried over MgSO4. The residue was concentrated under reduced pressure, dissolved in dichloromethane and passed through a short plug of silica gel (eluent was dichloromethane). The resulting material was used without further purification.
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In ethanol; water; toluene; for 18h;Inert atmosphere; Reflux; General procedure: To a solution of arylboronic acid (2.6 mmol), Na2CO3 (1.6 g, 15 mmol), and 2-bromopyridine (2.0 mmol) in toluene (7 mL)/ethanol (1.5 mL)/H2O (7 mL) was added Pd(PPh3)4 (0.069 g, 0.060 mmol) under argon. The reaction mixture was refluxed for 18 h, and then cooled to room temperature. To the reaction mixture was added aqueous NH4Cl (15 mL), extracted with EtOAc for three times, dried over Na2SO4, and evaporated in vacuumto afford the crude product, which was purified by flash chromatography on silica gel with hexane/EtOAc to give quantitative yield of corresponding aryl pyridines
 

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