Technology Process of C31H38Br2NO5(1+)*I(1-)
There total 8 articles about C31H38Br2NO5(1+)*I(1-) which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 2 steps
1: dmap; triethylamine / dichloromethane
2: potassium carbonate / acetonitrile / 5 h
With
dmap; potassium carbonate; triethylamine;
In
dichloromethane; acetonitrile;
DOI:10.1002/anie.201204274
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: sodium hydride / N,N-dimethyl-formamide; toluene / 0.5 h / 20 °C / Inert atmosphere
1.2: 0.5 h / Inert atmosphere
2.1: potassium carbonate / methanol / 1 h
3.1: Dess-Martin periodane / dichloromethane / 20 °C / Inert atmosphere
4.1: silver hexafluoroantimonate; (2R,5R)-5-benzyl-2-tert-butyl-3-methyl-imidazolidin-4-one hydrochloride / chloroform / 20 °C / Inert atmosphere
5.1: NaBH(OAc)3 / 1,2-dichloro-ethane / 20 °C / Inert atmosphere
6.1: lithium aluminium tetrahydride / tetrahydrofuran / 5 h / 20 °C / Inert atmosphere
7.1: dmap; triethylamine / dichloromethane
8.1: potassium carbonate / acetonitrile / 5 h
With
dmap; silver hexafluoroantimonate; lithium aluminium tetrahydride; (2R,5R)-5-benzyl-2-tert-butyl-3-methyl-imidazolidin-4-one hydrochloride; NaBH(OAc)3; sodium hydride; potassium carbonate; Dess-Martin periodane; triethylamine;
In
tetrahydrofuran; methanol; dichloromethane; chloroform; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene; acetonitrile;
4.1: Prins reaction;
DOI:10.1002/anie.201204274
- Guidance literature:
-
Multi-step reaction with 4 steps
1: NaBH(OAc)3 / 1,2-dichloro-ethane / 20 °C / Inert atmosphere
2: lithium aluminium tetrahydride / tetrahydrofuran / 5 h / 20 °C / Inert atmosphere
3: dmap; triethylamine / dichloromethane
4: potassium carbonate / acetonitrile / 5 h
With
dmap; lithium aluminium tetrahydride; NaBH(OAc)3; potassium carbonate; triethylamine;
In
tetrahydrofuran; dichloromethane; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1002/anie.201204274