Technology Process of C16H20O2
There total 1 articles about C16H20O2 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:
-
oct-7-en-1-yn-4-ol;
With
sodium hydride;
In
tetrahydrofuran; mineral oil;
at 0 - 23 ℃;
for 1.16667h;
Inert atmosphere;
p-Methoxybenzyl bromide;
In
tetrahydrofuran; mineral oil;
at 0 - 23 ℃;
for 18.1667h;
Inert atmosphere;
DOI:10.1016/j.tetlet.2011.06.114
- Guidance literature:
-
C16H20O2;
With
n-butyllithium;
In
tetrahydrofuran; hexane;
at -78 ℃;
for 0.166667h;
Inert atmosphere;
N-Methoxy-N-methylacetamide;
In
tetrahydrofuran; hexane;
at -78 - 23 ℃;
Inert atmosphere;
DOI:10.1016/j.tetlet.2011.06.114
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: n-butyllithium / tetrahydrofuran; hexane / 0.17 h / -78 °C / Inert atmosphere
1.2: -78 - 23 °C / Inert atmosphere
2.1: Grubbs catalyst first generation / benzene / 1 h / 23 °C / Inert atmosphere
3.1: methylaluminum dichloride / dichloromethane; toluene / 0.75 h / -78 °C / Inert atmosphere
4.1: osmium(VIII) oxide; water; 4-methylmorpholine N-oxide / tetrahydrofuran; tert-butyl alcohol / 15 h / 23 °C
5.1: pyridine; dmap / dichloromethane / 0.58 h / 0 °C / Inert atmosphere
6.1: Dess-Martin periodane / dichloromethane / 2 h / 23 °C / Inert atmosphere
7.1: water; potassium carbonate / methanol / 1 h / 23 °C
With
pyridine; Grubbs catalyst first generation; dmap; osmium(VIII) oxide; n-butyllithium; water; methylaluminum dichloride; potassium carbonate; Dess-Martin periodane; 4-methylmorpholine N-oxide;
In
tetrahydrofuran; methanol; hexane; dichloromethane; toluene; tert-butyl alcohol; benzene;
3.1: Diels-Alder reaction;
DOI:10.1016/j.tetlet.2011.06.114