Technology Process of dimethyl-thiocarbamic acid S-(4-bromo-3,5-dimethyl-phenyl) ester
There total 1 articles about dimethyl-thiocarbamic acid S-(4-bromo-3,5-dimethyl-phenyl) ester which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 2 steps
1: triethylamine / dmap / 1,4-dioxane / 20 h / Heating / reflux
2: tetradecane / Heating / reflux
With
triethylamine;
dmap;
In
1,4-dioxane; tetradecane;
- Guidance literature:
-
dimethyl-thiocarbamic acid S-(4-bromo-3,5-dimethyl-phenyl) ester;
With
sodium methylate;
In
methanol;
for 20h;
Inert atmosphere;
Reflux;
With
hydrogenchloride;
In
methanol; water;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: sodium methylate / methanol / 20 h / Heating / reflux
2.1: tributylphosphine; 1,1'-azodicarbonyl-dipiperidine / toluene / 0 - 20 °C
3.1: sodium hydroxide; water / tetrahydrofuran
4.1: 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine / dichloromethane / 20 °C
4.2: 20 °C
5.1: potassium fluoride / tetrakis(triphenylphosphine) palladium(0) / toluene / Heating / reflux
6.1: sodium hydroxide; water / tetrahydrofuran
With
4-methyl-morpholine; potassium fluoride; sodium hydroxide; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; tributylphosphine; water; sodium methylate; 1,1'-azodicarbonyl-dipiperidine;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran; methanol; dichloromethane; toluene;
2.1: Mitsunobu reaction / 5.1: Suzuki Coupling;