Technology Process of 2-iodo-3-methyl-4-nitrobenzoic acid
There total 5 articles about 2-iodo-3-methyl-4-nitrobenzoic acid which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
2-amino-3-methyl-4-nitrobenzoic acid;
With
phosphoric acid; sulfuric acid; sodium nitrite;
at 5 - 10 ℃;
for 0.5h;
With
copper(l) iodide; potassium iodide;
at 80 ℃;
for 0.166667h;
Further stages.;
DOI:10.1021/jm0702175
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: aq. NH2OH*HCl / ethanol / 1.5 h / Heating
2.1: aq. H2SO4 / 2.5 h / 93 °C
3.1: aq. H2O2; KOH; KCl / 2 h / 20 °C
4.1: NaNO2; aq. H2SO4; H3PO4 / 0.5 h / 5 - 10 °C
4.2: aq. KI; CuI / 0.17 h / 80 °C
With
potassium hydroxide; phosphoric acid; sulfuric acid; potassium chloride; hydroxylamine hydrochloride; dihydrogen peroxide; sodium nitrite;
In
ethanol;
DOI:10.1021/jm0702175
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: KHCO3 / CH2Cl2 / 1 h / 20 °C
2.1: aq. NH2OH*HCl / ethanol / 1.5 h / Heating
3.1: aq. H2SO4 / 2.5 h / 93 °C
4.1: aq. H2O2; KOH; KCl / 2 h / 20 °C
5.1: NaNO2; aq. H2SO4; H3PO4 / 0.5 h / 5 - 10 °C
5.2: aq. KI; CuI / 0.17 h / 80 °C
With
potassium hydroxide; phosphoric acid; sulfuric acid; potassium chloride; hydroxylamine hydrochloride; dihydrogen peroxide; potassium hydrogencarbonate; sodium nitrite;
In
ethanol; dichloromethane;
DOI:10.1021/jm0702175