Technology Process of C22H16F3N3O3
There total 5 articles about C22H16F3N3O3 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:
-
(R)-Styrene oxide; C13H10F3N3O2;
With
bismuth(III) chloride;
In
cyclohexane; acetonitrile;
at 60 ℃;
for 20h;
Sealed tube;
trimethyl orthoformate;
With
trifluoroacetic acid;
at 20 ℃;
for 1h;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: potassium carbonate / dimethyl sulfoxide / 100 °C
2.1: ammonia / methanol / 24 h / 100 °C / Sealed tube
3.1: hydrogen / Raney nickel / methanol / 24 h / 20 °C / 775.74 - 1034.32 Torr
4.1: bismuth(III) chloride / cyclohexane; acetonitrile / 20 h / 60 °C / Sealed tube
4.2: 1 h / 20 °C
With
bismuth(III) chloride; ammonia; hydrogen; potassium carbonate;
Raney nickel;
In
methanol; cyclohexane; dimethyl sulfoxide; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: ammonia / methanol / 24 h / 100 °C / Sealed tube
2.1: hydrogen / Raney nickel / methanol / 24 h / 20 °C / 775.74 - 1034.32 Torr
3.1: bismuth(III) chloride / cyclohexane; acetonitrile / 20 h / 60 °C / Sealed tube
3.2: 1 h / 20 °C
With
bismuth(III) chloride; ammonia; hydrogen;
Raney nickel;
In
methanol; cyclohexane; acetonitrile;