Technology Process of 6H-Benzo[b]fluorene, 7,8,9,11-tetrahydro-6,6,9,9-tetramethyl-
There total 1 articles about 6H-Benzo[b]fluorene, 7,8,9,11-tetrahydro-6,6,9,9-tetramethyl- 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:
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77308-48-6
1,1,4,4,7,7,10,10-octamethyl-2,3,4,7,8,9,10,12-octahydro-1H-dibenzo[b,h]fluorene
- Guidance literature:
-
aluminium trichloride;
In
dichloromethane;
Yield given. Yields of byproduct given;
0 deg C, 2 h, then rt, 24 h;
- Guidance literature:
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Multi-step reaction with 2 steps
1.1: n-butyllithium / hexane; diethyl ether / 4 h / 0 - 20 °C / Inert atmosphere; Schlenk technique
1.2: -78 - 20 °C / Inert atmosphere; Schlenk technique
2.1: n-butyllithium / hexane; diethyl ether / 3 h / 0 - 20 °C / Inert atmosphere; Schlenk technique
2.2: 0 - 20 °C / Inert atmosphere; Schlenk technique
With
n-butyllithium;
In
diethyl ether; hexane;
DOI:10.1016/j.jorganchem.2015.12.028
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: n-butyllithium / hexane; diethyl ether / 4 h / 0 - 20 °C / Inert atmosphere; Schlenk technique
1.2: -78 - 20 °C / Inert atmosphere; Schlenk technique
2.1: n-butyllithium / hexane; diethyl ether / 3 h / 0 - 20 °C / Inert atmosphere; Schlenk technique
2.2: 0 - 20 °C / Inert atmosphere; Schlenk technique
3.1: diethyl ether / 4 h / 20 °C / Inert atmosphere; Schlenk technique
3.2: 1 h / 20 °C / Inert atmosphere; Schlenk technique
3.3: 1 h / 20 °C / Inert atmosphere; Schlenk technique
With
n-butyllithium;
In
diethyl ether; hexane;
DOI:10.1016/j.jorganchem.2015.12.028