Technology Process of C27H24O4
There total 5 articles about C27H24O4 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:
-
With
diisobutylaluminium hydride;
In
tetrahydrofuran; hexane;
at -60 ℃;
for 3h;
Inert atmosphere;
DOI:10.1002/chem.201304092
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere
1.2: 1 h / -78 °C / Inert atmosphere
2.1: tetrahydrofuran; hexane / 11 h / 20 °C / Inert atmosphere
3.1: diisobutylaluminium hydride / tetrahydrofuran; hexane / 3 h / -60 °C / Inert atmosphere
With
n-butyllithium; diisobutylaluminium hydride;
In
tetrahydrofuran; hexane;
DOI:10.1002/chem.201304092
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: copper(l) iodide; triethylamine / 0.25 h / 23 °C / Inert atmosphere
1.2: 0.25 h / Inert atmosphere
1.3: 12 h / 20 °C / Inert atmosphere
2.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere
2.2: 1 h / -78 °C / Inert atmosphere
3.1: tetrahydrofuran; hexane / 11 h / 20 °C / Inert atmosphere
4.1: diisobutylaluminium hydride / tetrahydrofuran; hexane / 3 h / -60 °C / Inert atmosphere
With
copper(l) iodide; n-butyllithium; diisobutylaluminium hydride; triethylamine;
In
tetrahydrofuran; hexane;
1.1: |Sonogashira Cross-Coupling / 1.2: |Sonogashira Cross-Coupling / 1.3: |Sonogashira Cross-Coupling;
DOI:10.1002/chem.201304092