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Chemical Structure| 366-53-0 Chemical Structure| 366-53-0

Structure of 366-53-0

Chemical Structure| 366-53-0

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Product Details of [ 366-53-0 ]

CAS No. :366-53-0
Formula : C8H6F2N2O3
M.W : 216.14
SMILES Code : CC(NC1=CC(F)=C(C=C1F)[N+]([O-])=O)=O
MDL No. :MFCD18425996

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Application In Synthesis of [ 366-53-0 ]

* 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 [ 366-53-0 ]

[ 366-53-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 398-90-3 ]
  • [ 366-53-0 ]
YieldReaction ConditionsOperation in experiment
90.6% With nitric acid; for 2.0h; To a stirred HNCb solution (21.9 g, 333.27 mmol, 15.63 mL, 96% purity, 11.41 equiv) was added dropwise compound 3.2 (5.00 g, 29.22 mmol, 1 equiv) at 0 C. After addition was complete, the reaction mixture was stirred at 0 C for 2 hr. LC-MS and TLC (petroleum ether/ethyl acetate = 1/1, Rf = 0.61) showed compound 3.2 was consumed, and the main product was compound 3.3 (r.t. = 0.746 min, [M+H]+ = 216.7). The reaction mixture was poured into ice water (50 mL), stirred for 10 min and then filtered. The resulting cake was washed with water (50 mL x 3) and dried under reduced pressure to give compound 3.3 (5.72 g, 26.46 mmol, 90.6% yield) as a yellow solid. NMR (400 MHz DMSO-de): d 10.47 (br s, 1H), 8.36 (dd, J = 6.5, 14.1 Hz, 1H), 8.21 (dd, J = 7.0, 10.8 Hz, 1H), 2.20 (s, 3H).
88% With nitric acid; for 3.0h; Example 2 Synthesis of N-(2,5-difluoro-4-nitrophenyl)acetamide 12 To a stirred fuming nitric acid (90 mL) was added portion wise <strong>[398-90-3]N-(2,5-difluorophenyl)acetamide</strong> 11 (34.2 g, 0.2 mol) at 0 C. The resulting solution was stirred at 0 C. for 3 hours. The solution was poured into ice-water mixture. The resulting yellow solid was collected by filtration and washed with more water (3*50 mL), dried in vacuum, giving rise to the desired N-(2,5-difluoro-4-nitrophenyl)acetamide 12 as a pale yellow solid: 38.0 g (88%). 1H NMR (300 MHZ, DMSO-d6) δ 10.45 (s, 1H), 8.33 (dd, J1=6.3 Hz, J2=14.1 Hz, 1H), 8.19 (dd, J1=6.3 Hz, J2=14.1 Hz, 1H), 2.18 (s, 3H).
 

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