Technology Process of 4-(2-methoxy-5-methylphenyl)pentanal
There total 8 articles about 4-(2-methoxy-5-methylphenyl)pentanal 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
hexane; toluene;
at -70 ℃;
for 4h;
DOI:10.1002/jccs.200100128
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 70 percent / 80 percent phosphoric acid / toluene / 18 h / 20 °C
2.1: 92.6 percent / K2CO3 / acetone / 36 h / Heating
3.1: O3; sodium bicarbonate / CH2Cl2 / -78 - 0 °C
3.2: 50 percent / Et3N; Ac2O / CH2Cl2 / 4 h / 20 °C
4.1: 99 percent / BF3*Et2O / 15 h / 20 °C
5.1: 90 percent / Raney nickel / ethanol / 17 h / Heating
6.1: 91.7 percent / DIBAL-H / toluene; hexane / 4 h / -70 °C
With
phosphoric acid; boron trifluoride diethyl etherate; nickel; diisobutylaluminium hydride; sodium hydrogencarbonate; potassium carbonate; ozone;
In
ethanol; hexane; dichloromethane; acetone; toluene;
DOI:10.1002/jccs.200100128
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 92.6 percent / K2CO3 / acetone / 36 h / Heating
2.1: O3; sodium bicarbonate / CH2Cl2 / -78 - 0 °C
2.2: 50 percent / Et3N; Ac2O / CH2Cl2 / 4 h / 20 °C
3.1: 99 percent / BF3*Et2O / 15 h / 20 °C
4.1: 90 percent / Raney nickel / ethanol / 17 h / Heating
5.1: 91.7 percent / DIBAL-H / toluene; hexane / 4 h / -70 °C
With
boron trifluoride diethyl etherate; nickel; diisobutylaluminium hydride; sodium hydrogencarbonate; potassium carbonate; ozone;
In
ethanol; hexane; dichloromethane; acetone; toluene;
DOI:10.1002/jccs.200100128