Technology Process of 4-chloro-7-methoxy-3-(4-methoxyphenyl)isocoumarine
There total 3 articles about 4-chloro-7-methoxy-3-(4-methoxyphenyl)isocoumarine which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
5-methoxy-2-(4-methoxyphenylethynyl)benzoic acid methyl ester;
With
mercury(II) diacetate; acetic acid;
at 20 ℃;
for 1h;
With
copper(l) chloride;
In
tetrahydrofuran;
for 4h;
Heating;
DOI:10.1016/j.bmc.2005.07.014
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: 75 percent / triethylamine; CuI; tetrabutylammonium iodide / Pd(PPh3)4 / acetonitrile / 4 h / Heating
2.1: Hg(OAc)2; CH3CO2H / 1 h / 20 °C
2.2: 28 percent / CuCl / tetrahydrofuran / 4 h / Heating
With
copper(l) iodide; mercury(II) diacetate; tetra-(n-butyl)ammonium iodide; acetic acid; triethylamine;
tetrakis(triphenylphosphine) palladium(0);
In
acetonitrile;
1.1: Sonogashira coupling;
DOI:10.1016/j.bmc.2005.07.014
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: 90 percent / triethylamine / toluene / 1 h / 20 °C
2.1: 75 percent / triethylamine; CuI; tetrabutylammonium iodide / Pd(PPh3)4 / acetonitrile / 4 h / Heating
3.1: Hg(OAc)2; CH3CO2H / 1 h / 20 °C
3.2: 28 percent / CuCl / tetrahydrofuran / 4 h / Heating
With
copper(l) iodide; mercury(II) diacetate; tetra-(n-butyl)ammonium iodide; acetic acid; triethylamine;
tetrakis(triphenylphosphine) palladium(0);
In
toluene; acetonitrile;
2.1: Sonogashira coupling;
DOI:10.1016/j.bmc.2005.07.014