Technology Process of 1-methoxy-4-(19-methyleicos-19-enyl)benzene
There total 7 articles about 1-methoxy-4-(19-methyleicos-19-enyl)benzene 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
zirconocene dichloride;
In
dichloromethane;
for 12h;
DOI:10.1021/ja0300618
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 98 percent / I2; triphenylphosphine; imidazole / diethyl ether; acetonitrile / 0.5 h / 20 °C
2.1: Mg / tetrahydrofuran / 2 h / Heating
2.2: 49 percent / CuI / tetrahydrofuran / 16 h / 4 °C
3.1: 79 percent / tetrahydrofuran; dimethylsulfoxide / 2 h / 20 °C
4.1: 66 percent / Cp2ZrCl2 / CH2Cl2 / 12 h
With
1H-imidazole; zirconocene dichloride; iodine; magnesium; triphenylphosphine;
In
tetrahydrofuran; diethyl ether; dichloromethane; dimethyl sulfoxide; acetonitrile;
DOI:10.1021/ja0300618
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: (4,5-dihydro-N,N-Mes2-imidazole)Cl2Ru=C(H)-(o-O-iPr)C6H4 / 1,2-dichloro-ethane / 2 h
1.2: 92 percent / H2 / 1,2-dichloro-ethane / 12 h / 10343 Torr
2.1: K2CO3 / CH2Cl2; methanol / 6 h
3.1: 98 percent / I2; triphenylphosphine; imidazole / diethyl ether; acetonitrile / 0.5 h / 20 °C
4.1: Mg / tetrahydrofuran / 2 h / Heating
4.2: 49 percent / CuI / tetrahydrofuran / 16 h / 4 °C
5.1: 79 percent / tetrahydrofuran; dimethylsulfoxide / 2 h / 20 °C
6.1: 66 percent / Cp2ZrCl2 / CH2Cl2 / 12 h
With
1H-imidazole; zirconocene dichloride; (1,3-Bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(o-isopropoxyphenylmethylene)ruthenium; iodine; potassium carbonate; magnesium; triphenylphosphine;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; dimethyl sulfoxide; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1021/ja0300618