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Chemical Structure| 886762-35-2 Chemical Structure| 886762-35-2

Structure of 886762-35-2

Chemical Structure| 886762-35-2

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Product Details of [ 886762-35-2 ]

CAS No. :886762-35-2
Formula : C7H3F3INO3
M.W : 333.00
SMILES Code : FC(F)(F)OC1=CC=C(I)C([N+]([O-])=O)=C1
MDL No. :MFCD04039213

Safety of [ 886762-35-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 886762-35-2 ]

* 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 [ 886762-35-2 ]

[ 886762-35-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2267-23-4 ]
  • [ 886762-35-2 ]
YieldReaction ConditionsOperation in experiment
65% [Example 734] Compound q12 1-Iodo-2-nitro-4-(trifluoromethoxy)benzene [1549] sodium nitrite (378 mg, 5.48 mmol) were added to a mixture of <strong>[2267-23-4]2-nitro-4-(trifluoromethoxy)aniline</strong> (1.11 g, 4.98 mmol), a 35% aqueous hydrochloric acid solution (7.2 ml) and water (7.2 ml) under ice-cooling. After 20 minutes of stirring, acetic acid (5 ml) was added, and the mixture was stirred at room temperature for 20 minutes. Sodium nitrite (80.7 mg, 1.17 mmol) was added, and the mixture was stirred for 20 minutes under ice-cooling, after which potassium iodide (1.22 g, 7.38 mmol) dissolved in water (1.5 ml) was added, followed by 30 minutes of stirring. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was then washed with a saturated aqueous sodium thiosulfate solution, and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, followed by concentration under reduced pressure. The resultant residue was purified by silica gel column chromatography (ethyl acetate/n-hexane) to yield the title compound (1.07 g, 65%) as an orange oily substance. LCMS: m/z 334 [M+H]+ HPLC retention time: 0.90 min (analysis condition F)
65% The mixture of 2-nitro-4- (trifluoromethoxy) aniline (l.llg, 4.98mmol), 35% aqueous hydrochloric acid (7.2ml) and water (7.2ml) of, and under ice-cooling was added ice (8G ) and sodium nitrite (378mg, 5.48mmol), stirring for 20 minutes, acetic acid (5ml), stirred at room temperature for 20 minutes. Under ice-cooling, sodium nitrite (80.7mg, l_17mmol), stirred for 20 min, dissolved in water (1.5ml) of potassium iodide (1.22g, 7.38mmol), stirred for 30 minutes. The reaction mixture was added water, extracted with ethyl acetate, and the organic layer was washed with saturated aqueous sodium thiosulfate solution, and dried over anhydrous magnesium sulfate. After the drying agent was filtered off and concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography (ethyl acetate / n-hexane) to obtain the title compound (1.07g, 65%) of an orange oily substance.
 

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