Technology Process of C17H20F3NO3
There total 5 articles about C17H20F3NO3 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
trimethylsilyl iodide;
In
dichloromethane;
at 20 ℃;
for 2h;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: sodium hydroxide / tetrahydrofuran / 2 h / 20 °C
1.2: 0.33 h / 20 °C
1.3: Bargellini Reaction / 0 - 45 °C
2.1: diazomethyl-trimethyl-silane / acetonitrile; methanol / 0 - 20 °C
3.1: ChiralPak AD-5cm 20μm / hexane; isopropyl alcohol / 25 °C / Resolution of racemate
4.1: trimethylsilyl iodide / dichloromethane / 2 h / 20 °C
With
trimethylsilyl iodide; sodium hydroxide; diazomethyl-trimethyl-silane;
In
tetrahydrofuran; methanol; hexane; dichloromethane; isopropyl alcohol; acetonitrile;
1.1: |Bargellini Reaction / 1.2: |Bargellini Reaction;
DOI:10.1021/ml500019s
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: triethylamine / chloroform / 1 h / 0 - 20 °C
2.1: pyrrolidine / benzene / 20 °C / Inert atmosphere; Dean-Stark; Reflux
2.2: 70 °C / Inert atmosphere; Dean-Stark
3.1: sodium hydroxide / tetrahydrofuran / 2 h / 20 °C
3.2: 0.33 h / 20 °C
3.3: Bargellini Reaction / 0 - 45 °C
4.1: diazomethyl-trimethyl-silane / acetonitrile; methanol / 0 - 20 °C
5.1: ChiralPak AD-5cm 20μm / hexane; isopropyl alcohol / 25 °C / Resolution of racemate
6.1: trimethylsilyl iodide / dichloromethane / 2 h / 20 °C
With
pyrrolidine; trimethylsilyl iodide; triethylamine; sodium hydroxide; diazomethyl-trimethyl-silane;
In
tetrahydrofuran; methanol; hexane; dichloromethane; chloroform; isopropyl alcohol; acetonitrile; benzene;
3.1: |Bargellini Reaction / 3.2: |Bargellini Reaction;
DOI:10.1021/ml500019s