Technology Process of C26H27NO6
There total 7 articles about C26H27NO6 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:
-
C26H23NO6;
With
methylamine;
In
tetrahydrofuran; water;
at 21 - 23 ℃;
for 26h;
benzyl chloroformate;
With
potassium carbonate;
In
tetrahydrofuran; water;
at 20 ℃;
for 28h;
With
hydrogenchloride;
In
water;
pH=~ 5;
- Guidance literature:
-
C18H21NO4; benzyl chloroformate;
With
potassium carbonate;
In
tetrahydrofuran; water;
at 0 - 20 ℃;
for 28h;
With
hydrogenchloride;
In
water;
pH=~ 5;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: pyridine / isopropyl alcohol / 8 h / 80 - 82 °C
2.1: sodium hydride / tetra-(n-butyl)ammonium iodide / tetrahydrofuran; mineral oil / 18.5 h / -15 - 20 °C
3.1: ozone / dichloromethane / -70 °C
4.1: 2-methyl-but-2-ene; sodium hypochlorite; sodium dihydrogenphosphate / water; tert-butyl alcohol; tetrahydrofuran / 4 h / 10 - 20 °C
5.1: methylamine / water; tetrahydrofuran / 26 h / 5 - 23 °C
6.1: potassium carbonate / water; tetrahydrofuran / 28 h / 0 - 20 °C
6.2: pH ~ 5
With
sodium hypochlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; sodium hydride; potassium carbonate; ozone; methylamine;
pyridine; tetra-(n-butyl)ammonium iodide;
In
tetrahydrofuran; dichloromethane; water; isopropyl alcohol; mineral oil; tert-butyl alcohol;
4.1: Pinnick Oxidation;