Technology Process of 3-Buten-2-one, 3,4-diphenyl-, oxime
There total 10 articles about 3-Buten-2-one, 3,4-diphenyl-, oxime 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
hydroxylamine hydrochloride; sodium hydroxide;
In
methanol; water;
at 65 ℃;
for 1h;
DOI:10.1039/c4nj02075h
- Guidance literature:
-
With
hydroxylamine hydrochloride; sodium acetate;
In
methanol;
at 20 ℃;
Inert atmosphere;
DOI:10.1021/ol202176g
- Guidance literature:
-
Multi-step reaction with 4 steps
1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / 5 h / 20 °C / Inert atmosphere
2: [Rh(OH)(cod)]2; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / 1,4-dioxane; water / 3 h / 20 - 60 °C / Inert atmosphere
3: Dess-Martin periodane / dichloromethane / 0.17 h / 20 °C / Inert atmosphere
4: hydroxylamine hydrochloride; sodium acetate / methanol / 20 °C / Inert atmosphere
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; [Rh(OH)(cod)]2; hydroxylamine hydrochloride; sodium acetate; potassium carbonate; Dess-Martin periodane; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; triethylamine;
In
1,4-dioxane; methanol; dichloromethane; water;
1: Sonogashira coupling;
DOI:10.1021/ol202176g