Technology Process of ethyl 3-(4-methoxyphenyl)-4,4-dimethyl-3-vinylhept-6-enoate
There total 7 articles about ethyl 3-(4-methoxyphenyl)-4,4-dimethyl-3-vinylhept-6-enoate 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 6 steps
1.1: 85 percent / lithium / tetrahydrofuran / 1 h / sonication
2.1: 97 percent / pyridinium chlorochromate; silica gel / CH2Cl2 / 3 h / 20 °C
3.1: magnesium / tetrahydrofuran
3.2: 70 percent / tetrahydrofuran / 4 h / 20 °C
4.1: 83 percent / pyridinium chlorochromate; silica gel / CH2Cl2 / 30 h / 20 °C
5.1: 70 percent / sodium borohydride / methanol / 2 h / cooling
6.1: 47 percent / propionic acid / 48 h / 180 °C
With
sodium tetrahydroborate; silica gel; lithium; magnesium; propionic acid; pyridinium chlorochromate;
In
tetrahydrofuran; methanol; dichloromethane;
1.1: Barbier coupling / 6.1: Johnson-Claisen orthoester rearrangement;
DOI:10.1081/SCC-200034755
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 85 percent / lithium / tetrahydrofuran / 1 h / sonication
2.1: 97 percent / pyridinium chlorochromate; silica gel / CH2Cl2 / 3 h / 20 °C
3.1: magnesium / tetrahydrofuran
3.2: 70 percent / tetrahydrofuran / 4 h / 20 °C
4.1: 83 percent / pyridinium chlorochromate; silica gel / CH2Cl2 / 30 h / 20 °C
5.1: 70 percent / sodium borohydride / methanol / 2 h / cooling
6.1: 47 percent / propionic acid / 48 h / 180 °C
With
sodium tetrahydroborate; silica gel; lithium; magnesium; propionic acid; pyridinium chlorochromate;
In
tetrahydrofuran; methanol; dichloromethane;
1.1: Barbier coupling / 6.1: Johnson-Claisen orthoester rearrangement;
DOI:10.1081/SCC-200034755