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ethyl 3-{4-[2-(6-benzoylindol-1-yl)ethoxy]phenyl}-2-ethoxypropionate

Base Information
  • Chemical Name:ethyl 3-{4-[2-(6-benzoylindol-1-yl)ethoxy]phenyl}-2-ethoxypropionate
  • CAS No.:1433194-53-6
  • Molecular Formula:C30H31NO5
  • Molecular Weight:485.58
  • Hs Code.:
ethyl 3-{4-[2-(6-benzoylindol-1-yl)ethoxy]phenyl}-2-ethoxypropionate

Synonyms:ethyl 3-{4-[2-(6-benzoylindol-1-yl)ethoxy]phenyl}-2-ethoxypropionate

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Chemical Property of ethyl 3-{4-[2-(6-benzoylindol-1-yl)ethoxy]phenyl}-2-ethoxypropionate
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Technology Process of ethyl 3-{4-[2-(6-benzoylindol-1-yl)ethoxy]phenyl}-2-ethoxypropionate

There total 4 articles about ethyl 3-{4-[2-(6-benzoylindol-1-yl)ethoxy]phenyl}-2-ethoxypropionate 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:
6-indolyl phenyl ketone; With potassium carbonate; In N,N-dimethyl-formamide; at 100 ℃; for 1h;
ethyl 3-[4-(2-chloroethoxy)-phenyl]-2-ethoxy-propionate; In N,N-dimethyl-formamide; for 15h; Reflux;
DOI:10.1002/cmdc.201200316
Guidance literature:
Multi-step reaction with 2 steps
1.1: hydrogen; palladium 10% on activated carbon / ethanol / 20 h / 20 °C / 760.05 Torr
2.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 100 °C
2.2: 15 h / Reflux
With palladium 10% on activated carbon; hydrogen; potassium carbonate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1002/cmdc.201200316
Guidance literature:
Multi-step reaction with 2 steps
1.1: tetrahydrofuran; mineral oil; pentane / -78 - 20 °C
2.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 100 °C
2.2: 15 h / Reflux
With potassium carbonate; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil; pentane;
DOI:10.1002/cmdc.201200316
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