Technology Process of 1-azido-3-(azidomethyl)-5-cyanobenzene
There total 4 articles about 1-azido-3-(azidomethyl)-5-cyanobenzene which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
sodium azide;
In
N,N-dimethyl-formamide;
at 20 ℃;
Inert atmosphere;
DOI:10.1002/ejoc.201402516
- Guidance literature:
-
Multi-step reaction with 4 steps
1: (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine / hexane / 20 °C / Inert atmosphere
2: trimethylsilylazide; copper(l) chloride; potassium fluoride / methanol / 20 - 70 °C
3: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 3 h / 20 - 90 °C / Inert atmosphere
4: sodium azide / N,N-dimethyl-formamide / 20 °C / Inert atmosphere
With
potassium fluoride; N-Bromosuccinimide; sodium azide; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 2,2'-azobis(isobutyronitrile); trimethylsilylazide; 4,4'-di-tert-butyl-2,2'-bipyridine; copper(l) chloride;
In
methanol; tetrachloromethane; hexane; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.201402516
- Guidance literature:
-
Multi-step reaction with 2 steps
1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 3 h / 20 - 90 °C / Inert atmosphere
2: sodium azide / N,N-dimethyl-formamide / 20 °C / Inert atmosphere
With
N-Bromosuccinimide; sodium azide; 2,2'-azobis(isobutyronitrile);
In
tetrachloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.201402516
