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Chemical Structure| 14906-63-9 Chemical Structure| 14906-63-9

Structure of 14906-63-9

Chemical Structure| 14906-63-9

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Product Details of [ 14906-63-9 ]

CAS No. :14906-63-9
Formula : C8H9NO3
M.W : 167.16
SMILES Code : O=C(C1=C[N+]([O-])=CC=C1)OCC

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Application In Synthesis of [ 14906-63-9 ]

* 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 [ 14906-63-9 ]

[ 14906-63-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 14906-63-9 ]
  • [ 7677-24-9 ]
  • [ 76196-79-7 ]
  • [ 75358-90-6 ]
YieldReaction ConditionsOperation in experiment
5.7 g; 3.5 g [0141] To a solution of 3-ethoxycarbonylpyridine N-oxide in 330 mL of DCM were added trimethylsilyl cyanide (TMSCN) (1 1.0 g, 65.9 mmol, 1.0 eq) and dimethylcarbamoyl chloride (7.1 g, 65.9 mmol, 1.0 eq) and the reaction mixture was stirred at rt for 2 days. Then 10% K2C03 was slowly added to make the reaction mixture basic.Organic layer was separated, dried and evaporated to provide the crude, which was purified by column chromatography to provide compounds A (5.7 g) and B (3.5 g).
5.7 g; 3.5 g With potassium carbonate; N,N-Dimethylcarbamoyl chloride; In dichloromethane; at 20℃; for 48.0h; [0248] To a solution of 3-ethoxycarbonylpyridine N-oxide in 330 mL of DCM were added trimethylsilyl cyanide (TMSCN) (11.0 g, 65.9 mmol, 1.0 eq) and dimethylcarbamoyl chloride(7.1 g, 65.9 mmol, 1.0 eq) and the reaction mixture was stirred at rt for 2 days. Then 10% K2C03 was slowly added to make the reaction mixture basic. Organic layer was separated, dried and evaporated to provide the crude, which was purified by column chromatography to provide compounds A (5.7 g) and B (3.5 g).
5.7 g; 3.5 g With N,N-Dimethylcarbamoyl chloride; In dichloromethane; at 20℃; for 48.0h; To a solution of 3-ethoxycarbonylpyridine N-oxide in 330 mE of DCM were added trimethylsilyl cyanide (TMSCN) (11.0 g, 65.9 mmol, 1.0 eq) and dimethylcarbamoyl chloride (7.1 g, 65.9 mmol, 1.0 eq) and the reaction mixture was stirred at it for 2 days. Then 10% K2C03 was slowly added to make the reaction mixture basic. Organic layer was separated, dried and evaporated to provide the crude, which was purified by column chromatography to provide compounds A (5.7 g) and B (3.5 g).
  • 2
  • [ 14906-63-9 ]
  • [ 697739-12-1 ]
 

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