Technology Process of 3-tertbutyl-5-(cyclohexylmethyl)-6-phenyl-8-nitrophenanthridinium chloride
There total 7 articles about 3-tertbutyl-5-(cyclohexylmethyl)-6-phenyl-8-nitrophenanthridinium chloride 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:
-
C30H33FN2O2;
In
acetonitrile;
at 110 ℃;
for 1.5h;
Inert atmosphere;
Sealed tube;
Microwave irradiation;
With
hydrogenchloride;
In
diethyl ether;
DOI:10.1002/chem.201304241
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: nitrosonium tetrafluoroborate / dichloromethane / 13.5 h / 0 - 20 °C / Inert atmosphere
1.2: 2 h / Inert atmosphere; Reflux
2.1: n-butyllithium / tetrahydrofuran / 2.33 h / -77 °C
2.2: 14.17 h / -77 - 20 °C
2.3: 55 h
3.1: [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; N-ethyl-N,N-diisopropylamine / ethanol / 4 h / Inert atmosphere; Reflux
4.1: titanium tetrachloride / toluene / 20.08 h / 0 - 20 °C / Inert atmosphere
5.1: acetonitrile / 1.5 h / 110 °C / Inert atmosphere; Sealed tube; Microwave irradiation
With
n-butyllithium; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; titanium tetrachloride; nitrosonium tetrafluoroborate; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; ethanol; dichloromethane; toluene; acetonitrile;
1.1: |Balz-Schiemann Reaction / 3.1: |Suzuki-Miyaura Coupling;
DOI:10.1002/chem.201304241
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: n-butyllithium / tetrahydrofuran / 2.33 h / -77 °C
1.2: 14.17 h / -77 - 20 °C
1.3: 55 h
2.1: [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; N-ethyl-N,N-diisopropylamine / ethanol / 4 h / Inert atmosphere; Reflux
3.1: titanium tetrachloride / toluene / 20.08 h / 0 - 20 °C / Inert atmosphere
4.1: acetonitrile / 1.5 h / 110 °C / Inert atmosphere; Sealed tube; Microwave irradiation
With
n-butyllithium; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; titanium tetrachloride; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; ethanol; toluene; acetonitrile;
2.1: |Suzuki-Miyaura Coupling;
DOI:10.1002/chem.201304241