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Chemical Structure| 64326-17-6 Chemical Structure| 64326-17-6

Structure of 64326-17-6

Chemical Structure| 64326-17-6

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Product Details of [ 64326-17-6 ]

CAS No. :64326-17-6
Formula : C14H14O2
M.W : 214.26
SMILES Code : COC1=CC(OC)=CC(C2=CC=CC=C2)=C1
MDL No. :MFCD26383676

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Application In Synthesis of [ 64326-17-6 ]

* 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 [ 64326-17-6 ]

[ 64326-17-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 20469-65-2 ]
  • [ 98-80-6 ]
  • [ 64326-17-6 ]
YieldReaction ConditionsOperation in experiment
100% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; In 1,4-dioxane; water; at 90.0℃; for 4.0h;Inert atmosphere; a) 3,5-Dimethoxy-1,1'-biphenyl I115 A suspension of <strong>[20469-65-2]1-bromo-3,5-dimethoxybenzene</strong> (5.0 g, 23.0 mmol), phenylboronic acid (2.8 g, 23.0 mmol), Pd(dppf)Cl2 (0.57 g, 0.69 mmol) and potassium carbonate (4.8 g, 34.6 mmol) in 1,4-dioxane (80 ml.) and water (20 ml.) was heated at 90 C under N2 for 4 h. The mixture was diluted with water, extracted with EtOAc and the combined organic extracts were dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (Pet.ether/EtOAc = 500/1 to 200/1 to 100/1) to give the title compound (5.2 g, 100 %) as a white solid. LCMS-C: Rt 2.47 min; m/z 215.0 [M+H]+.
100% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; In 1,4-dioxane; water; at 90.0℃; for 4.0h;Inert atmosphere; A suspension of <strong>[20469-65-2]1-bromo-3,5-dimethoxybenzene</strong> (5.0 g, 23.0 mmol), phenylboronic acid (2.8 g, 23.0 mmol), Pd(dppf)Cl2 (0.57 g, 0.69 mmol) and potassium carbonate (4.8 g, 34.6 mmol) in 1,4-dioxane (80 ml.) and water (20 ml.) was heated at 90 C under N2 for 4 h. The mixture was diluted with water, extracted with EtOAc and the combined organic extracts were dried over Na2S04, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (petroleum ether/EtOAc = 500/1 to 200/1 to 100/1) to give the title compound 3,5-dimethoxy-1,1'-biphenyl I22 (5.2 g, 100 %) as a white solid. LCMS-A (ES-API): Rt 2.47 min; m/z 215.0 [M+H]+.
 

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