Technology Process of C29H45O9PSi
There total 14 articles about C29H45O9PSi 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:
-
dimethyl methane phosphonate;
With
n-butyllithium;
In
tetrahydrofuran;
at -78 ℃;
C26H36O6Si;
In
tetrahydrofuran;
DOI:10.1016/j.tetlet.2011.08.051
- Guidance literature:
-
Multi-step reaction with 10 steps
1: tert.-butyl lithium / tetrahydrofuran / -78 °C
2: zinc(II) tetrahydroborate / diethyl ether / -78 - -30 °C
3: tert.-butylhydroperoxide; bis(acetylacetonate)oxovanadium / dichloromethane / 0 - 24 °C
4: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran / 0 - 24 °C
5: tetrabutyl ammonium fluoride / tetrahydrofuran / 25 °C
6: lithium aluminium tetrahydride / tetrahydrofuran / -15 °C
7: 2,6-dimethylpyridine / dichloromethane / -40 °C
8: methanol; potassium carbonate / -15 °C
9: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 24 °C
10: n-butyllithium / tetrahydrofuran / -78 °C
With
2,6-dimethylpyridine; methanol; tert.-butylhydroperoxide; lithium aluminium tetrahydride; n-butyllithium; zinc(II) tetrahydroborate; bis(acetylacetonate)oxovanadium; tetrabutyl ammonium fluoride; tert.-butyl lithium; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane;
In
tetrahydrofuran; diethyl ether; dichloromethane;
9: Dess-Martin oxidation;
DOI:10.1016/j.tetlet.2011.08.051
- Guidance literature:
-
Multi-step reaction with 9 steps
1: zinc(II) tetrahydroborate / diethyl ether / -78 - -30 °C
2: tert.-butylhydroperoxide; bis(acetylacetonate)oxovanadium / dichloromethane / 0 - 24 °C
3: tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran / 0 - 24 °C
4: tetrabutyl ammonium fluoride / tetrahydrofuran / 25 °C
5: lithium aluminium tetrahydride / tetrahydrofuran / -15 °C
6: 2,6-dimethylpyridine / dichloromethane / -40 °C
7: methanol; potassium carbonate / -15 °C
8: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 24 °C
9: n-butyllithium / tetrahydrofuran / -78 °C
With
2,6-dimethylpyridine; methanol; tert.-butylhydroperoxide; lithium aluminium tetrahydride; n-butyllithium; zinc(II) tetrahydroborate; bis(acetylacetonate)oxovanadium; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane;
In
tetrahydrofuran; diethyl ether; dichloromethane;
8: Dess-Martin oxidation;
DOI:10.1016/j.tetlet.2011.08.051