Technology Process of 2-bromo-1-(2-chloro-4-(4-methoxyphenoxy)-6-methylphenyl)ethanone
There total 7 articles about 2-bromo-1-(2-chloro-4-(4-methoxyphenoxy)-6-methylphenyl)ethanone which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
tetra-N-butylammonium tribromide;
In
acetonitrile;
at 20 ℃;
for 0.5h;
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 2 h
2: aluminum (III) chloride / carbon disulfide / 4.5 h / 20 °C / Reflux
3: hydrogenchloride; water / 15 h / Reflux
4: potassium iodide; tert.-butylnitrite / acetonitrile / -10 - 20 °C
5: potassium phosphate; tetrabutylammomium bromide / copper(l) iodide / N,N-dimethyl-formamide / 22 h / Reflux
6: tetra-N-butylammonium tribromide / acetonitrile / 0.5 h / 20 °C
With
hydrogenchloride; potassium phosphate; tert.-butylnitrite; tetrabutylammomium bromide; water; tetra-N-butylammonium tribromide; potassium iodide;
aluminum (III) chloride; copper(l) iodide;
In
carbon disulfide; N,N-dimethyl-formamide; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 7 steps
1: tin(II) chloride dihdyrate / ethanol / 3 h / Reflux
2: 2 h
3: aluminum (III) chloride / carbon disulfide / 4.5 h / 20 °C / Reflux
4: hydrogenchloride; water / 15 h / Reflux
5: potassium iodide; tert.-butylnitrite / acetonitrile / -10 - 20 °C
6: potassium phosphate; tetrabutylammomium bromide / copper(l) iodide / N,N-dimethyl-formamide / 22 h / Reflux
7: tetra-N-butylammonium tribromide / acetonitrile / 0.5 h / 20 °C
With
hydrogenchloride; potassium phosphate; tert.-butylnitrite; tin(II) chloride dihdyrate; tetrabutylammomium bromide; water; tetra-N-butylammonium tribromide; potassium iodide;
aluminum (III) chloride; copper(l) iodide;
In
carbon disulfide; ethanol; N,N-dimethyl-formamide; acetonitrile;