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Chemical Structure| 122957-45-3 Chemical Structure| 122957-45-3

Structure of 122957-45-3

Chemical Structure| 122957-45-3

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Product Details of [ 122957-45-3 ]

CAS No. :122957-45-3
Formula : C7H8N2O3
M.W : 168.15
SMILES Code : O=C1C=C(C)NC(C)=C1[N+](=O)[O-]

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Application In Synthesis of [ 122957-45-3 ]

* 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 [ 122957-45-3 ]

[ 122957-45-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 122957-45-3 ]
  • [ 15513-48-1 ]
  • 2
  • [ 144-55-8 ]
  • [ 122957-45-3 ]
  • [ 15513-48-1 ]
YieldReaction ConditionsOperation in experiment
With trichlorophosphate; In dichloromethane; (b) 4-Chloro-2,6-dimethyl-3-nitropyridine By the method of Yakugaku Zasshi, 87, 387 (1967), 2,6-dimethyl-3-nitro-4-pyridone (11.23 g, 66.8 mmol) and phosphorus oxychloride (57 ml) were heated together at reflux for 11/2 hours. The excess reagent was removed under reduced pressure, and the residue dissolved in dichloromethane (150 ml). This solution was treated with dilute aqueous sodium bicarbonate until the aqueous layer was at pH7, and then the organic phase was separated, dried (MgSO4) and concentrated under reduced pressure to give a pale yellow solid, (9.8 g, 79percent). Caution: this compound is believed to be a powerful skin irritant. 1 H NMR (300 MHz, CDCl3) 2.58 (3H, s), 2.61 (3H, s), 7.22 (1H, s).
With trichlorophosphate; In dichloromethane; (b) 4-Chloro-2,6-dimethyl-3-nitropyridine By the method of Yakugaku Zasshi, 87, 387 (1967), 2,6-dimethyl-3-nitro-4(1H)-pyridone (see part (a)) (11.23 g, 66.8 mmol) and phosphorus oxychloride (57 ml) were heated together at reflux for 1.5 hours. The excess reagent was removed under reduced pressure, and the residue dissolved in dichloromethane (150 ml). This solution was treated with dilute aqueous sodium bicarbonate until the aqueous layer was at pH7, then the organic phase was separated, dried (MgSO4) and concentrated under reduced pressure to give the title compound as a pale yellow solid, (9.8 g, 79percent). Caution: this compound is a potential skin irritant. 1 H-NMR (300 MHz, CDCl3): delta=2.58 (3H, s), 2.61 (3H, s), 7.22 (1H, s) p.p.m.
With trichlorophosphate; In dichloromethane; (b) 4-Chloro-2,6-dimethyl-3-nitropyridine By the method of Yakugaku Zasshi , 87 , 387 (1967), 2,6-dimethyl-3-nitro-4-pyridone (11.23 g, 66.8 mmol) and phosphorus oxychloride (57 ml) were heated together at reflux for 1 1/2 hours. The excess reagent was removed under reduced pressure, and the residue dissolved in dichloromethane (150 ml). This solution was treated with dilute aqueous sodium bicarbonate until the aqueous layer was at pH7, and then the organic phase was separated, dried (MgSO4) and concentrated under reduced pressure to give a pale yellow solid, (9.8 g, 79percent). Caution: this compound is believed to be a powerful skin irritant. 1H NMR (300 MHz, CDCl3) 2.58 (3H, s), 2.61 (3H, s), 7.22 (1H, s).
 

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