Technology Process of (R)-1-ethyl-3-(3-fluorobenzyl)pyrrolidine
There total 5 articles about (R)-1-ethyl-3-(3-fluorobenzyl)pyrrolidine which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
potassium carbonate;
In
acetonitrile;
at 20 ℃;
for 2.5h;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 1H-imidazole; triphenylphosphine; iodine / 1,4-dioxane; diethyl ether / 20 °C / Cooling with ice
1.2: 20 °C
2.1: (1R,2R)-trans-2-aminocyclohexanol hydrochloride; sodium hexamethyldisilazane / nickel(I) iodide / isopropyl alcohol / 0.08 h / 40 °C / Sealed tube; Inert atmosphere
2.2: 70 °C
3.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
4.1: potassium carbonate / acetonitrile / 2.5 h / 20 °C
With
1H-imidazole; iodine; sodium hexamethyldisilazane; potassium carbonate; triphenylphosphine; (1R,2R)-trans-2-aminocyclohexanol hydrochloride; trifluoroacetic acid;
nickel(I) iodide;
In
1,4-dioxane; diethyl ether; dichloromethane; isopropyl alcohol; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: (1R,2R)-trans-2-aminocyclohexanol hydrochloride; sodium hexamethyldisilazane / nickel(I) iodide / isopropyl alcohol / 0.08 h / 40 °C / Sealed tube; Inert atmosphere
1.2: 70 °C
2.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
3.1: potassium carbonate / acetonitrile / 2.5 h / 20 °C
With
sodium hexamethyldisilazane; potassium carbonate; (1R,2R)-trans-2-aminocyclohexanol hydrochloride; trifluoroacetic acid;
nickel(I) iodide;
In
dichloromethane; isopropyl alcohol; acetonitrile;