Technology Process of 1-Methyl-1H-indole-3-carboxylic acid benzyl ester
There total 2 articles about 1-Methyl-1H-indole-3-carboxylic acid benzyl ester which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
bis-triphenylphosphine-palladium(II) chloride; oxygen; copper diacetate; dimethyl sulfoxide; triphenylphosphine;
In
toluene;
at 100 ℃;
for 36h;
under 760.051 Torr;
regioselective reaction;
DOI:10.1002/chem.201101300
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: potassium hydroxide / N,N-dimethyl-formamide
1.2: 20 °C
2.1: bis-triphenylphosphine-palladium(II) chloride; oxygen; copper diacetate; dimethyl sulfoxide; triphenylphosphine / toluene / 36 h / 100 °C / 760.05 Torr
With
bis-triphenylphosphine-palladium(II) chloride; oxygen; copper diacetate; dimethyl sulfoxide; triphenylphosphine; potassium hydroxide;
In
N,N-dimethyl-formamide; toluene;
DOI:10.1002/chem.201101300