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benzyl-(2-chloro-3-nitro-6-trifluoromethylpyridin-4-yl)amine

Base Information Edit
  • Chemical Name:benzyl-(2-chloro-3-nitro-6-trifluoromethylpyridin-4-yl)amine
  • CAS No.:947144-18-5
  • Molecular Formula:C13H9ClF3N3O2
  • Molecular Weight:331.682
  • Hs Code.:
  • Mol file:947144-18-5.mol
benzyl-(2-chloro-3-nitro-6-trifluoromethylpyridin-4-yl)amine

Synonyms:benzyl-(2-chloro-3-nitro-6-trifluoromethylpyridin-4-yl)amine

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Chemical Property of benzyl-(2-chloro-3-nitro-6-trifluoromethylpyridin-4-yl)amine Edit
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Technology Process of benzyl-(2-chloro-3-nitro-6-trifluoromethylpyridin-4-yl)amine

There total 5 articles about benzyl-(2-chloro-3-nitro-6-trifluoromethylpyridin-4-yl)amine 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:
4-(benzylamino)-3-nitro-6-(trifluoromethyl)pyridin-2-ol; With P,P-dichlorophenylphosphine oxide; at 100 ℃;
With sodium hydrogencarbonate; In water; ethyl acetate;
Guidance literature:
With P,P-dichlorophenylphosphine oxide; In dichloromethane; at 95 ℃; for 22h; Inert atmosphere; Large scale reaction;
DOI:10.1021/op200021a
Guidance literature:
Multi-step reaction with 5 steps
1: hydrogenchloride / water / Reflux
2: sulfuric acid; nitric acid / 5.5 h / 20 - 50 °C
3: P,P-dichlorophenylphosphine oxide / dichloromethane / 15 h / 95 °C / Inert atmosphere; Large scale reaction
4: tetrahydrofuran / 22 h / Reflux; Large scale reaction
5: P,P-dichlorophenylphosphine oxide / dichloromethane / 22 h / 95 °C / Inert atmosphere; Large scale reaction
With P,P-dichlorophenylphosphine oxide; hydrogenchloride; sulfuric acid; nitric acid; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/op200021a
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