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Chemical Structure| 863878-53-9 Chemical Structure| 863878-53-9

Structure of 863878-53-9

Chemical Structure| 863878-53-9

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Product Details of [ 863878-53-9 ]

CAS No. :863878-53-9
Formula : C22H21BO2
M.W : 328.21
SMILES Code : CC1(C)C(C)(C)OB(C2=CC=C3C4=CC=CC=C4C5=C3C2=CC=C5)O1
MDL No. :MFCD20527116

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Application In Synthesis of [ 863878-53-9 ]

* 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 [ 863878-53-9 ]

[ 863878-53-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 61676-62-8 ]
  • [ 13438-50-1 ]
  • [ 863878-53-9 ]
  • 2
  • [ 13438-50-1 ]
  • [ 73183-34-3 ]
  • [ 863878-53-9 ]
YieldReaction ConditionsOperation in experiment
76% With potassium acetate; bis(dibenzylideneacetone)-palladium(0); tricyclohexylphosphine; In 1,4-dioxane; for 3h;Reflux; To 100.00 g (1.0 eq) of <strong>[13438-50-1]3-bromofluoranthene</strong> was added 135.48 g of bis (pinacolato) diboron4.0 g (0.02 eq) of Pd (dba) 2, 3.8 g (0.04 eq) of PCy3 and 98.31 g (2.00 eq) of KOAc were placed in 800 mL of dioxane and the mixture was refluxed and stirred. After 3 hours, the solution was concentrated under reduced pressure. This was dissolved in CHCl3 and completely washed with water. The solution in which the product was dissolved was further concentrated under reduced pressure and purified by column chromatography. 88.72 g (yield 76percent) of Formula 2-3 was obtained
61% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; triethylamine; In 1,4-dioxane; at 75 - 80℃; To the flask was added 5.0 g (0.018 mol) of intermediate 10, 4.97 g (0.0196 mol) of PIN2B2, 0.44 g (0.54 mmol) of Pd (dppf)3.5 g (0.036 mol) of triethylamine and 90 ml of dioxane were added thereto, and the mixture was refluxed and stirred at 75 to 80 ° C under nitrogen for 2 hours. OnAfter the temperature was lowered to room temperature, the solvent was distilled off under reduced pressure. The resulting compound was purified by silica gel column chromatographyTo obtain 3.6 g (Yield: 61percent) of a pale yellow solid compound (Intermediate (11)).
 

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