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Chemical Structure| 1083171-75-8 Chemical Structure| 1083171-75-8

Structure of 1083171-75-8

Chemical Structure| 1083171-75-8

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Product Details of [ 1083171-75-8 ]

CAS No. :1083171-75-8
Formula : C12H19N3O
M.W : 221.30
SMILES Code : CC1=C(C)N=C(C)C(C=[N+]([O-])C(C)(C)C)=N1

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Application In Synthesis of [ 1083171-75-8 ]

* 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 [ 1083171-75-8 ]

[ 1083171-75-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 16649-50-6 ]
  • [ 186534-02-1 ]
  • [ 1083171-75-8 ]
YieldReaction ConditionsOperation in experiment
38% In methanol;Reflux; Example 1 Synthesis of TBN (FIG. 2) 2-[[(1,1-Dimethylethyl)oxidoimino]methyl]-3,5,6-trimethylpyrazine (TBN). To aldehyde 5 (1.9 g, 0.013 mol) in methanol (200 mL) was added tert-butylhydroxylamine (1 g, 0.011 mol), and the solution was refluxed for 2 h. Another portion of tert-butyl hydroxylamine (1 g, 0.011 mol) was then added, and the solution refluxed until aldehyde 5 was completely reacted. Solvent was removed in vacuo, and the product was extracted. The solution was dried with Na2SO4, and solvent removed in vacuo. The product was purified by column chromatography, eluding with ethyl acetate/petroleum ether (1/1, v/v), to produce TBN as a light yellow solid (1.1 g, 38% yield), mp: 68-70 C. 1H NMR (CDCl3, ppm): 7.82 (s, 1H), 2.47 (s, 3H), 2.50 (s, 3H), 2.52 (s, 3H), 1.63 (s, 9H). ESI-MS: 222 [M+H]+, 244 [M+Na]+. Anal. (C12H19N3O) C, H, N.
38% In mthanol;Reflux; To aldehyde 5 (1.9 g, 0.013 mol) in methanol (200 mL) was added tert-butylhydroxylamine (1 g, 0.011 mol), and the solution was refluxed for 2 h. Another portion of tert-butyl hydroxy lamine (1 g, 0.011 mol) was then added, and the solution refluxed until aldehyde 5 was completely reacted. Solvent was removed in vacuo, and the product was extracted. The solution was dried with Na2SO4, and solvent removed in vacuo. The product was purified by column chromatography, eluting with ethyl acetate/petroleum ether (1/1, v/v), to produce TBN as a light yellow solid (1.1 g, 38% yield), mp: 68-70 0C. 1H NMR (CDCl3, ppm): 7.82 (s, IH), 2.47 (s, 3H), 2.50 (s, 3H), 2.52 (s, 3H), 1.63 (s, 9H). ESI-MS: 222 [M+H]+, 244 [M+Na]+. Anal. (Ci2H19N3O) C, H, N.
 

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