Technology Process of C29H35NO8
There total 13 articles about C29H35NO8 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
dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
In
dichloromethane;
at 20 ℃;
DOI:10.1002/ejoc.201100034
- Guidance literature:
-
Multi-step reaction with 9 steps
1: N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 0 - 20 °C
2: water; 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 0.5 h / 20 °C
3: dmap; triethylamine / toluene / 16 h / 0 - 20 °C
4: hydrogenchloride; water / ethanol / 24 h / 20 °C
5: pyrrolidine; tetrakis(triphenylphosphine) palladium(0); triphenylphosphine / acetonitrile / 7 h / 0 - 20 °C
6: triphenylphosphine / toluene / 3 h / 20 °C
7: copper(I) trifluoromethanesulfonate benzene / benzene / 3 h / 80 °C
8: pyridine hydrogenfluoride / tetrahydrofuran / 3 h / 20 °C
9: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C
With
pyrrolidine; hydrogenchloride; dmap; tetrakis(triphenylphosphine) palladium(0); copper(I) trifluoromethanesulfonate benzene; water; pyridine hydrogenfluoride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; 2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
tetrahydrofuran; ethanol; dichloromethane; toluene; acetonitrile; benzene;
DOI:10.1002/ejoc.201100034
- Guidance literature:
-
Multi-step reaction with 8 steps
1: water; 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 0.5 h / 20 °C
2: dmap; triethylamine / toluene / 16 h / 0 - 20 °C
3: hydrogenchloride; water / ethanol / 24 h / 20 °C
4: pyrrolidine; tetrakis(triphenylphosphine) palladium(0); triphenylphosphine / acetonitrile / 7 h / 0 - 20 °C
5: triphenylphosphine / toluene / 3 h / 20 °C
6: copper(I) trifluoromethanesulfonate benzene / benzene / 3 h / 80 °C
7: pyridine hydrogenfluoride / tetrahydrofuran / 3 h / 20 °C
8: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C
With
pyrrolidine; hydrogenchloride; dmap; tetrakis(triphenylphosphine) palladium(0); copper(I) trifluoromethanesulfonate benzene; water; pyridine hydrogenfluoride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; triphenylphosphine; 2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
tetrahydrofuran; ethanol; dichloromethane; toluene; acetonitrile; benzene;
DOI:10.1002/ejoc.201100034