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C33H32N2O8

Base Information
  • Chemical Name:C33H32N2O8
  • CAS No.:1160950-97-9
  • Molecular Formula:C33H32N2O8
  • Molecular Weight:584.626
  • Hs Code.:
C<sub>33</sub>H<sub>32</sub>N<sub>2</sub>O<sub>8</sub>

Synonyms:

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Chemical Property of C33H32N2O8
Chemical Property:
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Technology Process of C33H32N2O8

There total 10 articles about C33H32N2O8 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 7 steps
1: pyridine / 12 h
2: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 12 h
3: triethylamine / tetrahydrofuran / 12 h
4: triethylamine / methanol / 12 h / 20 °C
5: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 0 °C
6: trifluoroacetic acid / dichloromethane / 12 h / 20 °C
7: pyridine
With di-isopropyl azodicarboxylate; palladium 10% on activated carbon; hydrogen; triethylamine; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; pyridine; methanol; dichloromethane; 5: Mitsunobu reaction;
DOI:10.1021/jm200148p
Guidance literature:
Multi-step reaction with 6 steps
1: thionyl chloride / tetrahydrofuran
2: triethylamine / tetrahydrofuran / 12 h
3: triethylamine / methanol / 12 h / 20 °C
4: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 0 °C
5: trifluoroacetic acid / dichloromethane / 12 h / 20 °C
6: pyridine
With thionyl chloride; di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; pyridine; methanol; dichloromethane; 4: Mitsunobu reaction;
DOI:10.1021/jm200148p
Guidance literature:
Multi-step reaction with 5 steps
1: triethylamine / tetrahydrofuran / 12 h
2: triethylamine / methanol / 12 h / 20 °C
3: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 0 °C
4: trifluoroacetic acid / dichloromethane / 12 h / 20 °C
5: pyridine
With di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; pyridine; methanol; dichloromethane; 3: Mitsunobu reaction;
DOI:10.1021/jm200148p
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