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Chemical Structure| 868406-81-9 Chemical Structure| 868406-81-9

Structure of 868406-81-9

Chemical Structure| 868406-81-9

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Product Details of [ 868406-81-9 ]

CAS No. :868406-81-9
Formula : C7H4BrClF3NO
M.W : 290.47
SMILES Code : NC1=CC(Cl)=C(OC(F)(F)F)C=C1Br
MDL No. :MFCD28734569

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Application In Synthesis of [ 868406-81-9 ]

* 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 [ 868406-81-9 ]

[ 868406-81-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64628-73-5 ]
  • [ 868406-81-9 ]
YieldReaction ConditionsOperation in experiment
42% With N-Bromosuccinimide; In dichloromethane; at 20℃; for 0.416667h; Example 35: (5-Chloro-2-f(E)-3-f3-(4-fluoro-benzvl)-3,8-diaza-bicvdoo3.2.11oct-8-yll-3-oxo- propenvll-4-trifluoromethoxv-phenyl)-urea; a) 2-Bromo-5-chloro-4-trifluoromethoxy-phenylamine; N-Bromosuccinimid (7.9 g; 44.5 mmol) in CH2CI2 (500 ml) is added under stirring within 5 min. to a solution of <strong>[64628-73-5]3-chloro-4-trifluoromethoxy-phenylamine</strong> (9.4 g; 44.5 mmol) in CH2CI2 (100 ml) at room temp. After 20 min. the reaction mixture is concentrated to a volume of -150 ml, and hexanes (1000 ml) added to the precipitated crystals. The crystals are filtered off an purified via chromatography (Si02; TBME/hexanes 1/9 to 2/8) to deliver the target compound as yellowish crystals (8.4 g; 42 %). 1 H-NMR (400MHz; DMSO-d6), 8 (ppm) : 5.81 (s, 1 H); 6.94 (s, 1 H); 7.55 (s, 2H). MS (m/z) ES-: 290 (MH-).
 

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