Technology Process of C36H66O7Si2
There total 5 articles about C36H66O7Si2 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
2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
dichloromethane;
at 0 ℃;
for 1h;
Molecular sieve;
Inert atmosphere;
DOI:10.1039/c2ob25100k
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: triethylamine; (-)-diisopinocamphenylborane chloride / diethyl ether / 1 h / -78 - 0 °C / Inert atmosphere
1.2: 17 h / -78 - -20 °C / Inert atmosphere
2.1: acetic acid; tetramethylammonium triacetoxyborohydride / acetonitrile / 21 h / -30 - -20 °C / Inert atmosphere
3.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 1 h / 0 °C / Molecular sieve; Inert atmosphere
With
acetic acid; triethylamine; (-)-diisopinocamphenylborane chloride; 2,3-dicyano-5,6-dichloro-p-benzoquinone; tetramethylammonium triacetoxyborohydride;
In
diethyl ether; dichloromethane; acetonitrile;
1.1: Aldol condensation / 1.2: Aldol condensation;
DOI:10.1039/c2ob25100k
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: ozone / dichloromethane / -78 °C / Inert atmosphere
1.2: 4 h / -78 - 20 °C / Inert atmosphere
2.1: triethylamine; (-)-diisopinocamphenylborane chloride / diethyl ether / 1 h / -78 - 0 °C / Inert atmosphere
2.2: 17 h / -78 - -20 °C / Inert atmosphere
3.1: acetic acid; tetramethylammonium triacetoxyborohydride / acetonitrile / 21 h / -30 - -20 °C / Inert atmosphere
4.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 1 h / 0 °C / Molecular sieve; Inert atmosphere
With
ozone; acetic acid; triethylamine; (-)-diisopinocamphenylborane chloride; 2,3-dicyano-5,6-dichloro-p-benzoquinone; tetramethylammonium triacetoxyborohydride;
In
diethyl ether; dichloromethane; acetonitrile;
2.1: Aldol condensation / 2.2: Aldol condensation;
DOI:10.1039/c2ob25100k