Technology Process of C47H64N2O6
There total 5 articles about C47H64N2O6 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride;
In
toluene;
at 50 ℃;
for 4h;
Inert atmosphere;
DOI:10.1002/chem.201100180
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 4-methyl-morpholine; benzotriazol-1-ol / dichloromethane / 0 °C / Inert atmosphere
1.2: 16 h / 20 °C / Inert atmosphere
2.1: tetrakis(triphenylphosphine) palladium(0); copper(I) thiophene-2-carboxylate; Tetrabutylammoniumsalz der Diphenylphosphinsaeure / N,N-dimethyl-formamide / 0.17 h / Inert atmosphere
3.1: 4-pyrrolidin-1-ylpyridine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.17 h / 0 - 20 °C / Inert atmosphere
3.2: 18 h / Inert atmosphere
4.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / toluene / 4 h / 50 °C / Inert atmosphere
With
4-methyl-morpholine; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; tetrakis(triphenylphosphine) palladium(0); copper(I) thiophene-2-carboxylate; benzotriazol-1-ol; 4-pyrrolidin-1-ylpyridine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; Tetrabutylammoniumsalz der Diphenylphosphinsaeure;
In
dichloromethane; N,N-dimethyl-formamide; toluene;
2.1: Stille coupling;
DOI:10.1002/chem.201100180
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: tetraethylammonium fluoride / acetonitrile / 16 h / 40 °C / Inert atmosphere
2.1: 4-methyl-morpholine; benzotriazol-1-ol / dichloromethane / 0 °C / Inert atmosphere
2.2: 16 h / 20 °C / Inert atmosphere
3.1: tetrakis(triphenylphosphine) palladium(0); copper(I) thiophene-2-carboxylate; Tetrabutylammoniumsalz der Diphenylphosphinsaeure / N,N-dimethyl-formamide / 0.17 h / Inert atmosphere
4.1: 4-pyrrolidin-1-ylpyridine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.17 h / 0 - 20 °C / Inert atmosphere
4.2: 18 h / Inert atmosphere
5.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / toluene / 4 h / 50 °C / Inert atmosphere
With
4-methyl-morpholine; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; tetrakis(triphenylphosphine) palladium(0); copper(I) thiophene-2-carboxylate; tetraethylammonium fluoride; benzotriazol-1-ol; 4-pyrrolidin-1-ylpyridine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; Tetrabutylammoniumsalz der Diphenylphosphinsaeure;
In
dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;
3.1: Stille coupling;
DOI:10.1002/chem.201100180