Technology Process of 3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid
There total 4 articles about 3-chloro-4-(6-methoxyquinolin-2-yl)benzoic acid which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate;
In
water;
at 110 ℃;
for 3h;
Inert atmosphere;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: acetic anhydride / 2 h / Reflux
2: trichlorophosphate / 2 h / Reflux
3: potassium carbonate; 2-(2-methoxyethoxy)ethyl alcohol / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / water / 3 h / 110 °C / Inert atmosphere
With
2-(2-methoxyethoxy)ethyl alcohol; acetic anhydride; potassium carbonate; trichlorophosphate;
(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride;
In
water;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: dihydrogen peroxide / water; acetic acid / 21 h / 70 °C
1.2: pH 8 - 9
2.1: acetic anhydride / 2 h / Reflux
3.1: trichlorophosphate / 2 h / Reflux
4.1: potassium carbonate; 2-(2-methoxyethoxy)ethyl alcohol / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / water / 3 h / 110 °C / Inert atmosphere
With
2-(2-methoxyethoxy)ethyl alcohol; dihydrogen peroxide; acetic anhydride; potassium carbonate; trichlorophosphate;
(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride;
In
water; acetic acid;