Technology Process of 4-iodo-3-methoxyphenylacetic acid
There total 1 articles about 4-iodo-3-methoxyphenylacetic acid 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:
-
methyl 4-iodo-3-methoxyphenylacetate;
With
potassium hydroxide;
In
methanol;
at 90 ℃;
for 3h;
Reflux;
Inert atmosphere;
With
hydrogenchloride;
In
methanol; water;
Inert atmosphere;
DOI:10.1021/jm301127x
- Guidance literature:
-
Multi-step reaction with 2 steps
1: palladium diacetate; sodium carbonate; tetrabutylammomium bromide / water / 120 °C / Microwave irradiation; Inert atmosphere
2: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 24 h / 0 - 20 °C / Inert atmosphere
With
4-methyl-morpholine; tetrabutylammomium bromide; palladium diacetate; sodium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
In
dichloromethane; water;
1: |Suzuki Coupling;
DOI:10.1021/jm301127x
- Guidance literature:
-
Multi-step reaction with 3 steps
1: palladium diacetate; sodium carbonate; tetrabutylammomium bromide / water / 120 °C / Microwave irradiation; Inert atmosphere
2: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 24 h / 0 - 20 °C / Inert atmosphere
3: boron tribromide / dichloromethane / 0 - 20 °C / Inert atmosphere
With
4-methyl-morpholine; tetrabutylammomium bromide; palladium diacetate; boron tribromide; sodium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
In
dichloromethane; water;
1: |Suzuki Coupling;
DOI:10.1021/jm301127x