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Chemical Structure| 191846-76-1 Chemical Structure| 191846-76-1

Structure of 191846-76-1

Chemical Structure| 191846-76-1

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Product Details of [ 191846-76-1 ]

CAS No. :191846-76-1
Formula : C11H10N2O4
M.W : 234.21
SMILES Code : O=CC1=CN(C)C2=C1C([N+]([O-])=O)=C(OC)C=C2
MDL No. :MFCD03093098

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Application In Synthesis of [ 191846-76-1 ]

* 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 [ 191846-76-1 ]

[ 191846-76-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 39974-94-2 ]
  • [ 191846-76-1 ]
YieldReaction ConditionsOperation in experiment
73% With nitric acid; acetic acid; To a solution of 23 (1.02 g, 5.39 mmol) dissolved in AcOH (88.7 mL) was added a mixture of concentrated HNO3 (3.2 mL in 18 mL AcOH) dropwise at 0 C over 1 h. After addition, the mixture was stirred at room temperature for 2 h, added to crushed ice (75 g), filtered, washed with H2O and dried to give 24 (0.90 g, 70%) as a pale yellow solid. 1H NMR (300 MHz, DMSO-d6): delta (ppm) 9.72 (s, 1H), 8.45 (s,1H), 7.82 (d, J = 9.1 Hz, 1H), 7.37 (d, J = 9.1 Hz, 1H), 3.93 (s, 3H), 3.91 (s, 3H); MS (ESI) m/z: 235.0 [M+H]+.
With nitric acid; acetic acid; at 10 - 20℃; for 16h; To a solution of the starting aldehyde (29.5 g, 156 mmol, 1 eq.) 5-methoxy-1-methyl-1H- indole-3-carbaldehyde in acetic acid (300 mL), cooled to 10C. To this, a mixture of nitric acid(4.6 mL) in acetic acid (20 mL) was added. The reaction mixture was then stirred at rt for 16 h. A yellow suspension was obtained which was poured on to an ice-water mixture and the crystals obtained were filtered off and dried. Crude product was triturated from EAHex to afford product as a yellow solid (30.0 g, 82.1%)
 

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