Technology Process of (R)-3-phenyl-1,2,3,4-tetrahydroisoquinoline
There total 8 articles about (R)-3-phenyl-1,2,3,4-tetrahydroisoquinoline 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
chloro(1,5-cyclooctadiene)rhodium(I) dimer; ZhaoPhos; hydrogen;
In
dichloromethane; isopropyl alcohol;
at 25 ℃;
for 48h;
under 30402 Torr;
enantioselective reaction;
DOI:10.1039/c5sc04712a
- Guidance literature:
-
(R)-2-[2-(hydroxymethyl)phenyl]-1-phenylethanamine;
With
thionyl chloride;
In
chloroform;
at 0 - 50 ℃;
With
sodium hydroxide;
In
tetrahydrofuran; water;
at 20 ℃;
for 10h;
DOI:10.1002/ejoc.201000111
- Guidance literature:
-
1-<2-((tert-butoxycarbonyl)aminomethyl)phenyl>-1-phenylethanone;
With
bis(1,5-cyclooctadiene)diiridium(I) dichloride; C46H38FeP2; trifluoroacetic acid;
In
dichloromethane;
for 3h;
With
hydrogen;
In
dichloromethane; toluene;
at 50 ℃;
for 24h;
under 38002.6 Torr;
Reagent/catalyst;
Overall yield = 70 percent; enantioselective reaction;
Molecular sieve;
DOI:10.1039/d0cy01271h
