Technology Process of 2-Hepten-1-ol, 7-[(4-methoxyphenyl)methoxy]-, (2E)-
There total 13 articles about 2-Hepten-1-ol, 7-[(4-methoxyphenyl)methoxy]-, (2E)- 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
diisobutylaluminium hydride;
In
dichloromethane; cyclohexane;
at -78 ℃;
for 0.333333h;
DOI:10.1021/ol051415y
- Guidance literature:
-
methyl (E)-7-(4-methoxybenzyloxy)hept-2-enoate;
With
diisobutylaluminium hydride;
In
tetrahydrofuran; hexane;
at -78 - 20 ℃;
for 4h;
Inert atmosphere;
With
methanol;
In
tetrahydrofuran; hexane;
at -78 - 20 ℃;
Inert atmosphere;
DOI:10.1039/c7ob00079k
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: 100 percent / oxalyl chloride; DMSO; triethylamine / CH2Cl2 / -78 - 22 °C
2.1: sodium hydride / tetrahydrofuran / 1 h / 0 °C
2.2: 91 percent / tetrahydrofuran / 0.33 h / 22 °C
3.1: 100 percent / diisobutylaluminum hydride / cyclohexane; CH2Cl2 / 0.33 h / -78 °C
With
oxalyl dichloride; sodium hydride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine;
In
tetrahydrofuran; dichloromethane; cyclohexane;
1.1: Swern oxidation / 2.2: Horner-Emmons reaction;
DOI:10.1021/ol051415y