Technology Process of 6,6-dichlorofulvene
There total 1 articles about 6,6-dichlorofulvene which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
oxygen;
Further byproducts given. Title compound not separated from byproducts;
Formation of xenobiotics;
combustion;
DOI:10.1016/S0045-6535(00)00216-2
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: aluminum (III) chloride / tetrahydrofuran / 5 h / -9 °C / Inert atmosphere
1.2: 0.5 h / -9 °C
2.1: hydrogen / rhodium contaminated with carbon / water; tetrahydrofuran / 7 h
3.1: sodium tetrahydroborate; methanol / tetrahydrofuran / 1.5 h / 0 - 5 °C
4.1: sulfuric acid / 0.67 h / 20 °C
5.1: hydroxylamine hydrochloride; pyridine / ethanol / 4 h / 20 °C
6.1: triethylamine / 1,4-dioxane / 3 h / 25 - 82 °C
6.2: 0.5 h
With
pyridine; methanol; sodium tetrahydroborate; sulfuric acid; hydroxylamine hydrochloride; hydrogen; triethylamine;
aluminum (III) chloride; rhodium contaminated with carbon;
In
tetrahydrofuran; 1,4-dioxane; ethanol; water;
- Guidance literature:
-
Multi-step reaction with 6 steps
1: aluminum (III) chloride / toluene; tetrahydrofuran / 5 h / -9 °C / Inert atmosphere
2: hydrogen / 5% Rh/C / water; tetrahydrofuran / 7 h / Inert atmosphere
3: sodium tetrahydroborate / tetrahydrofuran; methanol / 1.5 h / 0 - 5 °C
4: sulfuric acid / 0.67 h / 20 °C
5: hydroxylamine hydrochloride; pyridine / ethanol / 4 h / 20 °C
6: triethylamine / 1,4-dioxane / 3 h / 82 °C
With
pyridine; sodium tetrahydroborate; sulfuric acid; hydroxylamine hydrochloride; hydrogen; triethylamine;
aluminum (III) chloride; 5% Rh/C;
In
tetrahydrofuran; 1,4-dioxane; methanol; ethanol; water; toluene;
1: Diels-Alder Reaction;