Technology Process of meso-(1R,4aR,5as,6aS,10S,10aS,11as,12aR)-1,10-bis(3-(2-phenylethenyl)phenyl)-octadecahydronaphthacene
There total 5 articles about meso-(1R,4aR,5as,6aS,10S,10aS,11as,12aR)-1,10-bis(3-(2-phenylethenyl)phenyl)-octadecahydronaphthacene 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:
-
O,O-diethyl benzylphosphonate;
With
sodium hydride;
In
1,2-dimethoxyethane; hexane;
at 20 ℃;
for 3h;
meso-(1R,4aR,5as,6aS,10S,10aS,11as,12aR)-1,10-bis(3-formylphenyl)-octadecahydronaphthacene;
In
1,2-dimethoxyethane; hexane;
at 20 ℃;
for 20h;
Further stages.;
DOI:10.1021/ol9913439
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 1.67 g / ethanol / Raney nikel / 24 h / Heating
2.1: N-bromosuccinimide; α,α-azobisisobutyronitrile / CCl4 / 0.17 h / Heating
3.1: calcium carbonate; water / dioxane / 19 h / 20 °C
4.1: 491 mg / pyridinium chlorochromate / CH2Cl2 / 2 h / 20 °C
5.1: sodium hydride / 1,2-dimethoxy-ethane; hexane / 3 h / 20 °C
5.2: 70 percent / 1,2-dimethoxy-ethane; hexane / 20 h / 20 °C
With
N-Bromosuccinimide; ethanol; azobisisobutyronitrile; water; sodium hydride; pyridinium chlorochromate; calcium carbonate;
Raney nikel;
In
1,4-dioxane; tetrachloromethane; 1,2-dimethoxyethane; hexane; dichloromethane;
1.1: Hydrogenolysis / 2.1: Bromination / 3.1: Hydrolysis / 4.1: Oxidation / 5.1: Substitution / 5.2: Condensation;
DOI:10.1021/ol9913439
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: N-bromosuccinimide; α,α-azobisisobutyronitrile / CCl4 / 0.17 h / Heating
2.1: calcium carbonate; water / dioxane / 19 h / 20 °C
3.1: 491 mg / pyridinium chlorochromate / CH2Cl2 / 2 h / 20 °C
4.1: sodium hydride / 1,2-dimethoxy-ethane; hexane / 3 h / 20 °C
4.2: 70 percent / 1,2-dimethoxy-ethane; hexane / 20 h / 20 °C
With
N-Bromosuccinimide; azobisisobutyronitrile; water; sodium hydride; pyridinium chlorochromate; calcium carbonate;
In
1,4-dioxane; tetrachloromethane; 1,2-dimethoxyethane; hexane; dichloromethane;
1.1: Bromination / 2.1: Hydrolysis / 3.1: Oxidation / 4.1: Substitution / 4.2: Condensation;
DOI:10.1021/ol9913439