Technology Process of 1H-3-Benzazepin-1-ol,
2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-3-methyl-2-phenyl-
There total 4 articles about 1H-3-Benzazepin-1-ol,
2,3,4,5-tetrahydro-1-(4-hydroxyphenyl)-3-methyl-2-phenyl- 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:
-
Multi-step reaction with 4 steps
1: 43.3 percent / benzyltrimethyl-ammonium tribromide / CH2Cl2; methanol / 5 h / Heating
2: 83.3 percent / propylene oxide / dioxane / 1.5 h / 110 °C
3: 50 percent / n-C4H9Li / hexane; tetrahydrofuran / 0.5 h / 20 °C
4: 58.5 percent / TBAF / tetrahydrofuran / 0.5 h / cooling
With
n-butyllithium; benzyltrimethylammonium tribromide; tetrabutyl ammonium fluoride; methyloxirane;
In
tetrahydrofuran; 1,4-dioxane; methanol; hexane; dichloromethane;
3: intramolecular Barbier reaction;
DOI:10.3987/com-06-10853
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 50 percent / n-C4H9Li / hexane; tetrahydrofuran / 0.5 h / 20 °C
2: 58.5 percent / TBAF / tetrahydrofuran / 0.5 h / cooling
With
n-butyllithium; tetrabutyl ammonium fluoride;
In
tetrahydrofuran; hexane;
1: intramolecular Barbier reaction;
DOI:10.3987/com-06-10853
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 96.4 percent / imidazole / CH2Cl2 / 2 h / 20 °C
2: 43.3 percent / benzyltrimethyl-ammonium tribromide / CH2Cl2; methanol / 5 h / Heating
3: 83.3 percent / propylene oxide / dioxane / 1.5 h / 110 °C
4: 50 percent / n-C4H9Li / hexane; tetrahydrofuran / 0.5 h / 20 °C
5: 58.5 percent / TBAF / tetrahydrofuran / 0.5 h / cooling
With
1H-imidazole; n-butyllithium; benzyltrimethylammonium tribromide; tetrabutyl ammonium fluoride; methyloxirane;
In
tetrahydrofuran; 1,4-dioxane; methanol; hexane; dichloromethane;
4: intramolecular Barbier reaction;
DOI:10.3987/com-06-10853