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Chemical Structure| 930791-49-4 Chemical Structure| 930791-49-4

Structure of 930791-49-4

Chemical Structure| 930791-49-4

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Product Details of [ 930791-49-4 ]

CAS No. :930791-49-4
Formula : C12H9FN2O2
M.W : 232.21
SMILES Code : O=[N+](C1=C(F)C=CC=C1NC2=CC=CC=C2)[O-]
MDL No. :MFCD17519587

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Application In Synthesis of [ 930791-49-4 ]

* 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 [ 930791-49-4 ]

[ 930791-49-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19064-24-5 ]
  • [ 62-53-3 ]
  • [ 930791-49-4 ]
YieldReaction ConditionsOperation in experiment
78% With potassium tert-butylate; In N,N-dimethyl-formamide; at 20℃; for 16h; Step 1 To a solution of <strong>[19064-24-5]2,6-difluoronitrobenzene</strong> (2.0 g, 6.28 mmol) and aniline (d 1.022, 1.15 mL, 12.6 mmol) in dry N,N-dimethylformamide (10 mL) was added potassium tert-butoxide (1.40 g, 12.5 mmol) in portions. After 16 hours at room temperature, the reaction mixture was poured into saturated aqueous ammonium chloride solution and extracted with dichloromethane (2*50 mL). The combined organic layers were washed with water (1*50 mL), dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford crude 3-fluoro-2-nitro-N-phenylaniline (1.15 g, 78%), which was used in the next step without further purification.
73% Step 1: (3-Fluoro-2-nitrophenyl)phenylamine Sodium tertbutoxide (1.2 g, 12.58 mmol) was added portionwise to a stirred solution of <strong>[19064-24-5]1,3-difluoro-2-nitrobenzene</strong> (1 g, 6.29 mmol) and phenylamine (1.15 mL, 12.58 mmol) in a hydrous DMF (5 mL) under a nitrogen atmosphere at RT and stirring was continued for 20 h. The mixture was poured into an aqueous solution of NH4Cl and extracted with EtOAc (150 mL). The organic layer was washed with brine, then dried and concentrated in vacuo and the resulting residue was purified by column chromatography (Si-PCC, gradient 0-15% EtOAc in cyclohexane) affording (3-Fluoro-2-nitrophenyl)phenylamine as a red solid (1.06 g, 73%). LCMS: RT 3.80 min.
With potassium fluoride; In dimethyl sulfoxide; at 95℃; for 15h; (1) Add aniline (3.3mL, 36.2mmol), <strong>[19064-24-5]2,6-difluoronitrobenzene</strong> (3mL, 30mmol) and anhydrous potassium fluoride (1.8g, 30mmol) to 9mL of dimethyl sulfoxide and stir After the dissolution is complete, react at 95C for 15 hours; after the reaction is complete, cool the system to room temperature, then add 30mL of distilled water to the reaction system, stir until a large amount of red precipitate appears, filter the precipitate and wash with 30ml (10ml×3 times) distilled water 3 times The filtered solid is dried in a drying box to obtain intermediate product A;
 

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