Technology Process of C42H58O7Si
There total 10 articles about C42H58O7Si 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:
-
acetic acid methyl ester;
With
lithium diisopropyl amide;
In
tetrahydrofuran;
at -78 ℃;
C39H52O5Si;
In
tetrahydrofuran;
at -78 ℃;
DOI:10.1016/j.tetlet.2012.01.058
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: toluene-4-sulfonic acid / benzene / Reflux
2.1: n-butyllithium / tetrahydrofuran / -78 °C
2.2: -78 - 20 °C
3.1: sodium bis(2-methoxyethoxy)aluminium dihydride / diethyl ether / 20 °C
3.2: 0 °C
3.3: -78 °C
4.1: 1H-imidazole / dichloromethane / 20 °C
5.1: tetrakis(triphenylphosphine) palladium(0); triethylamine / 60 °C
6.1: diisobutylaluminium hydride / dichloromethane / -78 °C
7.1: hydrogenchloride; water / tetrahydrofuran / 20 °C
8.1: N-ethyl-N,N-diisopropylamine / 1,2-dichloro-ethane / 50 °C
9.1: lithium diisopropyl amide / tetrahydrofuran / -78 °C
9.2: -78 °C
With
1H-imidazole; hydrogenchloride; tetrakis(triphenylphosphine) palladium(0); n-butyllithium; water; diisobutylaluminium hydride; toluene-4-sulfonic acid; triethylamine; N-ethyl-N,N-diisopropylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; lithium diisopropyl amide;
In
tetrahydrofuran; diethyl ether; dichloromethane; 1,2-dichloro-ethane; benzene;
DOI:10.1016/j.tetlet.2012.01.058
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: N-ethyl-N,N-diisopropylamine / 1,2-dichloro-ethane / 50 °C
2.1: lithium diisopropyl amide / tetrahydrofuran / -78 °C
2.2: -78 °C
With
N-ethyl-N,N-diisopropylamine; lithium diisopropyl amide;
In
tetrahydrofuran; 1,2-dichloro-ethane;
DOI:10.1016/j.tetlet.2012.01.058