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Chemical Structure| 1255208-55-9 Chemical Structure| 1255208-55-9

Structure of 1255208-55-9

Chemical Structure| 1255208-55-9

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Product Details of [ 1255208-55-9 ]

CAS No. :1255208-55-9
Formula : C8H6N2O
M.W : 146.15
SMILES Code : C=CC1=CC2=NON=C2C=C1
MDL No. :MFCD26401745

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Application In Synthesis of [ 1255208-55-9 ]

* 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 [ 1255208-55-9 ]

[ 1255208-55-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 51376-06-8 ]
  • potassium vinyltrifluoroborate [ No CAS ]
  • [ 1255208-55-9 ]
YieldReaction ConditionsOperation in experiment
With triethylamine;dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In ethanol; for 3h;Reflux; 5-Brorno-2,l,3-benzoxadiazole (5.5 g, 27.6 mmol)), potassium vinylfluoroborate (7.40 g, 55.3 mmol), and PdC12(dppi>;CH2C12Adduct (1.088 g, 1.332 mmol) were suspended in ethanol (75 ml) then added TEA (7.70 ml, 55.3 mmol). The reaction mixture was then degassed and heated to reflux for 3hrs. The reaction was diluted with ethyl acetate and washed with brine. The organic layer was dried over Na2SO4, filtered and evaporated to dryness. The residue was purified through a 330g ISCO Redi-Sep silica gel plug and eluted with 20%ETOAc/hexane to yield 5- ethenyl-2 , 1 , 3 -benzoxadiazole.1H-NMR (600 MHz5 CDCl3): delta ppm 7.81(d, J=9.3 Hz, IH), 7.66 (s, IH), 7.63 (d, J-9.3 Hz, IHX 6.35 (d, J=10.9 Hz, 0.5H), 6.80 (d, J-10.9 Hz, 0.5H)s 5.94 (d. J-17.5 Hz, IH)5 5.55 (d, J= H Hz5 IH).
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; triethylamine; In ethanol; at 80℃; for 12h; Step A: 5-ethenyl-2, 1 ,3-benzoxadiazole: 5-bromo-2, 1 ,3-benzoxadiazole (4.0 g, 20 mmol),potassium vinyltrifluoroborate (5.40 g, 40.2 mmol) and Pd(dppf)Clr (1.6 g, 2 mmol) in TEA (5.2mL) and EtOH (15 mL) were added to a flask containing a stir bar, and the flask was then heated at 80 C for 12h. The organic residue was dissolved in EtOAc (500 mL) and the solution was washed with brine, dried over sodium sulfate, filtered and concentrated. The resulting organic residue was subjected to purification over silica gel to give the title compound.
 

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