Technology Process of Boronic acid, (5-chloro-2-ethylphenyl)-
There total 5 articles about Boronic acid, (5-chloro-2-ethylphenyl)- which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
4-chloro-1-ethyl-2-iodobenzene;
With
isopropylmagnesium chloride;
In
tetrahydrofuran;
at -30 ℃;
for 0.5h;
Inert atmosphere;
Trimethyl borate;
In
tetrahydrofuran;
at -30 ℃;
for 1.5h;
With
hydrogenchloride; water;
In
tetrahydrofuran;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: nitric acid; sulfuric acid / 1 h / -5 - 10 °C
2.1: hydrogenchloride; sodium nitrite / water / 1.5 h / 0 °C
2.2: 2 h / 20 - 80 °C
3.1: hydrazine hydrate; iron(III) chloride / methanol / 13 h / Reflux
4.1: aniline; toluene-4-sulfonic acid; potassium iodide; sodium nitrite / water / 0.5 h
5.1: isopropylmagnesium chloride / tetrahydrofuran / 0.5 h / -30 °C / Inert atmosphere
5.2: 1.5 h / -30 °C
With
hydrogenchloride; iron(III) chloride; sulfuric acid; isopropylmagnesium chloride; nitric acid; toluene-4-sulfonic acid; hydrazine hydrate; aniline; potassium iodide; sodium nitrite;
In
tetrahydrofuran; methanol; water;
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: aniline; toluene-4-sulfonic acid; potassium iodide; sodium nitrite / water / 0.5 h
2.1: isopropylmagnesium chloride / tetrahydrofuran / 0.5 h / -30 °C / Inert atmosphere
2.2: 1.5 h / -30 °C
With
isopropylmagnesium chloride; toluene-4-sulfonic acid; aniline; potassium iodide; sodium nitrite;
In
tetrahydrofuran; water;