Technology Process of C33H48O10
There total 3 articles about C33H48O10 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
1,1'-bis-(diphenylphosphino)ferrocene; (η4-1,5-cyclooctadiene)dichlororuthenium(II); potassium carbonate;
In
acetonitrile;
at 60 ℃;
for 48h;
Inert atmosphere;
DOI:10.1002/anie.201302543
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / toluene / 96 h / 20 °C
1.2: 24 h
2.1: potassium carbonate; 1,1'-bis-(diphenylphosphino)ferrocene; (η4-1,5-cyclooctadiene)dichlororuthenium(II) / acetonitrile / 48 h / 60 °C / Inert atmosphere
With
1,1'-bis-(diphenylphosphino)ferrocene; (η4-1,5-cyclooctadiene)dichlororuthenium(II); potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
toluene; acetonitrile;
1.1: |Baylis-Hillman Reaction;
DOI:10.1002/anie.201302543
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: triethylamine; tetrabutyl-ammonium chloride / dichloromethane / 0.25 h / 0 °C / Molecular sieve
1.2: 3.25 h / 0 - 20 °C / Molecular sieve
2.1: potassium carbonate; 1,1'-bis-(diphenylphosphino)ferrocene; (η4-1,5-cyclooctadiene)dichlororuthenium(II) / acetonitrile / 48 h / 60 °C / Inert atmosphere
With
1,1'-bis-(diphenylphosphino)ferrocene; (η4-1,5-cyclooctadiene)dichlororuthenium(II); tetrabutyl-ammonium chloride; potassium carbonate; triethylamine;
In
dichloromethane; acetonitrile;
DOI:10.1002/anie.201302543