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trans-2,6-dimethyl-2-nitrocyclohexanone

Base Information
  • Chemical Name:trans-2,6-dimethyl-2-nitrocyclohexanone
  • CAS No.:80594-91-8
  • Molecular Formula:C8H13NO3
  • Molecular Weight:171.196
  • Hs Code.:
trans-2,6-dimethyl-2-nitrocyclohexanone

Synonyms:

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Chemical Property of trans-2,6-dimethyl-2-nitrocyclohexanone
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Technology Process of trans-2,6-dimethyl-2-nitrocyclohexanone

There total 5 articles about trans-2,6-dimethyl-2-nitrocyclohexanone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 2 steps
1: 52 percent Chromat. / triethylamine / dimethylformamide / 120 h / 110 °C
2: 8.5 percent / NO2BF4 / acetonitrile / 1.) -25 deg C, 1 h, 2.) RT, 2 h
With nitronium tetrafluoborate; triethylamine; In N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jo00346a006
Guidance literature:
Multi-step reaction with 2 steps
1: NO2BF4 / acetonitrile / 1.) -25 deg C, 1 h, 2.) RT, 3 h
2: 1.) n-butylliyhium, diisopropylamine, hexamethylphosphoric triamide / 1.) THF, -78 deg C, 30 min, 2a.) -78 deg C, 30 min, 2b.) from 0 deg C to 10 deg C, 3 h
With N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium; nitronium tetrafluoborate; diisopropylamine; In acetonitrile;
DOI:10.1021/jo00346a006
Guidance literature:
Multi-step reaction with 2 steps
1: 21 percent / conc. aq. HNO3, acetic anhydride / 2 h / 15 - 22 °C
2: 1.) n-butylliyhium, diisopropylamine, hexamethylphosphoric triamide / 1.) THF, -78 deg C, 30 min, 2a.) -78 deg C, 30 min, 2b.) from 0 deg C to 10 deg C, 3 h
With N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium; nitric acid; acetic anhydride; diisopropylamine;
DOI:10.1021/jo00346a006
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