Technology Process of 6,7-bisbenzyloxy-1-(3,4-bisbenzyloxybenzyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride
There total 7 articles about 6,7-bisbenzyloxy-1-(3,4-bisbenzyloxybenzyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride 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 tetrahydroborate;
In
methanol;
at 0 ℃;
for 0.75h;
DOI:10.1039/P19810002016
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 70 percent / lithium aluminium hydride / tetrahydrofuran / 1.25 h / Heating
2: sodium hydrogen carbonate / CH2Cl2; H2O / 1.5 h
3: 85 percent / phosphorus oxychloride / acetonitrile / 0.42 h / Heating
4: 92 percent / sodium borohydride / methanol / 0.75 h / 0 °C
With
sodium tetrahydroborate; lithium aluminium tetrahydride; sodium hydrogencarbonate; trichlorophosphate;
In
tetrahydrofuran; methanol; dichloromethane; water; acetonitrile;
DOI:10.1039/P19810002016
- Guidance literature:
-
Multi-step reaction with 4 steps
1: oxalyl chloride, DMF / benzene / 1 h / 20 °C
2: sodium hydrogen carbonate / CH2Cl2; H2O / 1.5 h
3: 85 percent / phosphorus oxychloride / acetonitrile / 0.42 h / Heating
4: 92 percent / sodium borohydride / methanol / 0.75 h / 0 °C
With
sodium tetrahydroborate; oxalyl dichloride; sodium hydrogencarbonate; N,N-dimethyl-formamide; trichlorophosphate;
In
methanol; dichloromethane; water; acetonitrile; benzene;
DOI:10.1039/P19810002016