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C34H40N2O4

Base Information
  • Chemical Name:C34H40N2O4
  • CAS No.:1447825-73-1
  • Molecular Formula:C34H40N2O4
  • Molecular Weight:540.703
  • Hs Code.:
C<sub>34</sub>H<sub>40</sub>N<sub>2</sub>O<sub>4</sub>

Synonyms:

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Chemical Property of C34H40N2O4
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Technology Process of C34H40N2O4

There total 9 articles about C34H40N2O4 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 9 steps
1.1: diisobutylaluminium hydride / dichloromethane; toluene / 0.33 h / -78 °C
1.2: 1 h / 20 °C
2.1: copper(II) sulfate / dichloromethane / 22 h / 20 °C
3.1: tetrahydrofuran; dichloromethane / 0.67 h / 20 °C
4.1: hydrogenchloride / methanol; ethyl acetate / 5 h / 20 °C
5.1: sodium carbonate / tetrahydrofuran; water / 12 h / 20 °C
6.1: Dess-Martin periodane / dichloromethane / 0.5 h / 20 °C
7.1: 2-methyl-but-2-ene; sodium dihydrogenphosphate dihydrate; sodium chlorite / tetrahydrofuran; tert-butyl alcohol; water / 14 h / 20 °C
8.1: triethylamine; diphenyl phosphoryl azide / dichloromethane / 17.33 h / 0 - 20 °C
9.1: 29 h / Reflux
With hydrogenchloride; sodium chlorite; sodium dihydrogenphosphate dihydrate; 2-methyl-but-2-ene; diphenyl phosphoryl azide; diisobutylaluminium hydride; sodium carbonate; Dess-Martin periodane; copper(II) sulfate; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; toluene; tert-butyl alcohol; 3.1: |Grignard Reaction / 6.1: |Dess-Martin Oxidation / 9.1: |Curtius Rearrangement;
DOI:10.1021/jm400542h
Guidance literature:
Multi-step reaction with 6 steps
1: hydrogenchloride / methanol; ethyl acetate / 5 h / 20 °C
2: sodium carbonate / tetrahydrofuran; water / 12 h / 20 °C
3: Dess-Martin periodane / dichloromethane / 0.5 h / 20 °C
4: 2-methyl-but-2-ene; sodium dihydrogenphosphate dihydrate; sodium chlorite / tetrahydrofuran; tert-butyl alcohol; water / 14 h / 20 °C
5: triethylamine; diphenyl phosphoryl azide / dichloromethane / 17.33 h / 0 - 20 °C
6: 29 h / Reflux
With hydrogenchloride; sodium chlorite; sodium dihydrogenphosphate dihydrate; 2-methyl-but-2-ene; diphenyl phosphoryl azide; sodium carbonate; Dess-Martin periodane; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; tert-butyl alcohol; 3: |Dess-Martin Oxidation / 6: |Curtius Rearrangement;
DOI:10.1021/jm400542h
Guidance literature:
Multi-step reaction with 7 steps
1: tetrahydrofuran; dichloromethane / 0.67 h / 20 °C
2: hydrogenchloride / methanol; ethyl acetate / 5 h / 20 °C
3: sodium carbonate / tetrahydrofuran; water / 12 h / 20 °C
4: Dess-Martin periodane / dichloromethane / 0.5 h / 20 °C
5: 2-methyl-but-2-ene; sodium dihydrogenphosphate dihydrate; sodium chlorite / tetrahydrofuran; tert-butyl alcohol; water / 14 h / 20 °C
6: triethylamine; diphenyl phosphoryl azide / dichloromethane / 17.33 h / 0 - 20 °C
7: 29 h / Reflux
With hydrogenchloride; sodium chlorite; sodium dihydrogenphosphate dihydrate; 2-methyl-but-2-ene; diphenyl phosphoryl azide; sodium carbonate; Dess-Martin periodane; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; tert-butyl alcohol; 1: |Grignard Reaction / 4: |Dess-Martin Oxidation / 7: |Curtius Rearrangement;
DOI:10.1021/jm400542h
upstream raw materials:

C33H39NO4Si

C27H39NO2SSi

C35H49NO2SSi

C23H30O2Si

Downstream raw materials:

C25H37N3O4

C33H43N3O6

C30H41N3O5

C30H36N2O3

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