Technology Process of C30H52O6Si
There total 8 articles about C30H52O6Si 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
N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at 0 - 20 ℃;
Inert atmosphere;
DOI:10.1016/j.tet.2011.02.061
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: sodium hydroxide / tetrahydrofuran; water / 40 °C
1.2: 20 °C
2.1: triethyl borane; oxygen; tri-n-butyl-tin hydride / toluene / -30 °C
3.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere
4.1: dmap; triethylamine / dichloromethane / -10 °C / Inert atmosphere
5.1: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 20 °C
6.1: sodium tetrahydroborate / methanol / -10 °C
7.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
With
dmap; sodium tetrahydroborate; lithium aluminium tetrahydride; triethyl borane; oxygen; tri-n-butyl-tin hydride; sodium hydrogencarbonate; Dess-Martin periodane; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide;
In
tetrahydrofuran; methanol; dichloromethane; water; toluene;
DOI:10.1016/j.tet.2011.02.061
- Guidance literature:
-
Multi-step reaction with 4 steps
1: dmap; triethylamine / dichloromethane / -10 °C / Inert atmosphere
2: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 20 °C
3: sodium tetrahydroborate / methanol / -10 °C
4: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
With
dmap; sodium tetrahydroborate; sodium hydrogencarbonate; Dess-Martin periodane; triethylamine; N-ethyl-N,N-diisopropylamine;
In
methanol; dichloromethane;
DOI:10.1016/j.tet.2011.02.061