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(E)-N-(1-ethoxy-1-oxopropan-2-ylidene)-1,1-diphenylmethanamine oxide

Base Information
  • Chemical Name:(E)-N-(1-ethoxy-1-oxopropan-2-ylidene)-1,1-diphenylmethanamine oxide
  • CAS No.:1416475-89-2
  • Molecular Formula:C18H19NO3
  • Molecular Weight:297.354
  • Hs Code.:
(E)-N-(1-ethoxy-1-oxopropan-2-ylidene)-1,1-diphenylmethanamine oxide

Synonyms:(E)-N-(1-ethoxy-1-oxopropan-2-ylidene)-1,1-diphenylmethanamine oxide

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Chemical Property of (E)-N-(1-ethoxy-1-oxopropan-2-ylidene)-1,1-diphenylmethanamine oxide
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Technology Process of (E)-N-(1-ethoxy-1-oxopropan-2-ylidene)-1,1-diphenylmethanamine oxide

There total 3 articles about (E)-N-(1-ethoxy-1-oxopropan-2-ylidene)-1,1-diphenylmethanamine oxide 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 3 steps
1.1: N-ethyl-N,N-diisopropylamine; tetra-(n-butyl)ammonium iodide / acetonitrile / 72 h / 20 °C / Inert atmosphere
2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.5 h / 0 - 20 °C / Inert atmosphere
2.2: 0.33 h / Inert atmosphere
3.1: sodium acetate trihydrate / methanol / 20 °C / Inert atmosphere
With sodium acetate trihydrate; tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.tetasy.2012.11.010
Guidance literature:
Multi-step reaction with 2 steps
1.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.5 h / 0 - 20 °C / Inert atmosphere
1.2: 0.33 h / Inert atmosphere
2.1: sodium acetate trihydrate / methanol / 20 °C / Inert atmosphere
With sodium acetate trihydrate; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane;
DOI:10.1016/j.tetasy.2012.11.010
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