Technology Process of 4-<2-(Diethylamino)ethoxy>-1,2-dimethyl-1,4-cyclohexadien
There total 2 articles about 4-<2-(Diethylamino)ethoxy>-1,2-dimethyl-1,4-cyclohexadien 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
ammonia; lithium;
In
diethyl ether; tert-butyl alcohol;
at -45 ℃;
for 2h;
Yield given;
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 1.) 80percent NaOH / 1.) paraffin oil, toluene, 30 min, reflux, 2.) toluene, 4 h, reflux
2: 61 percent / NH3, Li / 2-methyl-propan-2-ol; diethyl ether / 2 h / -45 °C
With
sodium hydroxide; ammonia; lithium;
In
diethyl ether; tert-butyl alcohol;
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 1.) 15percent BuLi / 1.) n-hexane, THF, -80 deg C, 15 min, 2.) HMPA, -70 deg C
2: 6 N HCl / acetone / 2 h / 0 deg C up to room temp.
3: 94 percent / p-toluenesulfonic acid / diethyl ether / 2 h / Ambient temperature
4: 94 percent / LiAlH4 / diethyl ether / 1 h / Ambient temperature
5: 92 percent / KOH / dimethylsulfoxide / 2 h / Ambient temperature
6: 77 percent Turnov. / NH3, Li / diethyl ether / 1 h / -45 °C
7: 96 percent / 1N HCl / ethanol / 1 h / 50 °C
8: 73 percent / Jones-reagent (CrO3) / acetone / 0 °C
With
chromium(VI) oxide; hydrogenchloride; potassium hydroxide; lithium aluminium tetrahydride; n-butyllithium; ammonia; lithium;
toluene-4-sulfonic acid;
In
diethyl ether; ethanol; dimethyl sulfoxide; acetone;