Technology Process of C30H29Cl5N2O8
There total 10 articles about C30H29Cl5N2O8 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
boron trifluoride diethyl etherate;
In
dichloromethane;
at 0 - 20 ℃;
chemoselective reaction;
DOI:10.1016/j.tet.2012.03.121
- Guidance literature:
-
With
hydrogen fluoride;
In
acetonitrile;
at 20 ℃;
for 5h;
chemoselective reaction;
DOI:10.1016/j.tet.2012.03.121
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: lithium borohydride / tetrahydrofuran / 0 - 20 °C
2.1: sodium hydride / tetrahydrofuran; mineral oil / 0 °C
2.2: 3 h / 0 °C
3.1: sulfuryl dichloride / dichloromethane / 1 h / 20 °C
4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 0 °C
5.1: 1H-imidazole / dichloromethane / 4 h
6.1: N-Bromosuccinimide; boron trifluoride diethyl etherate / acetonitrile / 0.25 h / 20 °C / Darkness
7.1: hydrogen fluoride / acetonitrile / 5 h / 20 °C
With
1H-imidazole; N-Bromosuccinimide; lithium borohydride; sulfuryl dichloride; boron trifluoride diethyl etherate; hydrogen fluoride; sodium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile; mineral oil;
DOI:10.1016/j.tet.2012.03.121