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Chemical Structure| 383-08-4 Chemical Structure| 383-08-4

Structure of 383-08-4

Chemical Structure| 383-08-4

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Product Details of [ 383-08-4 ]

CAS No. :383-08-4
Formula : C9H5F5N2
M.W : 236.14
SMILES Code : FC(C1=NC2=CC=CC=C2N1)(F)C(F)(F)F
MDL No. :MFCD07779575

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Application In Synthesis of [ 383-08-4 ]

* 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 [ 383-08-4 ]

[ 383-08-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 422-64-0 ]
  • [ 95-54-5 ]
  • [ 383-08-4 ]
YieldReaction ConditionsOperation in experiment
100% for 4h;Reflux; To a 50 mL eggplant-shaped flask equipped with a magnetic stirrer, 3.2 g (30 mmol) of 1,2-phenylenediamine and 9.8 g (60 mmol) of <strong>[422-64-0]pentafluoropropionic acid</strong> were added. The mixture was heated to reflux for 4 hours. After cooling, the reaction mixture was poured into an aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to obtain 7.3 g of crystals. Yield: 100%. 1H-NMR (400 MHz, CDCl3, relative to TMS) delta (ppm): 7.43 (m, 2H), 7.58 (m, 1H), 7.92 (m, 1H), 9.87 (br, 1H).
99% at 70℃; for 16h; General procedure: In a screw-cap vial, the diamine or aminothiophenol (1 mmol) was dissolved in fluorinated carboxylic acid (2 mL, 0.5 M) and the reaction was stirred at 70 C for 16 hours. The fluorinated carboxylic acid was then evaporated under reduced pressure and the crude product was purified by silica gel column chromatography to yield the corresponding product.
 

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