Technology Process of 2-Cyclohexene-1-acetyl chloride, 1-ethyl-
There total 2 articles about 2-Cyclohexene-1-acetyl chloride, 1-ethyl- 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
oxalyl dichloride;
In
dichloromethane;
for 2h;
Heating;
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 94.4 percent / aq. KOH / methanol / 2 h / Heating
2: 88.6 percent / oxalyl chloride / CH2Cl2 / 2 h / Heating
With
potassium hydroxide; oxalyl dichloride;
In
methanol; dichloromethane;
-
-
103557-92-2,142560-76-7
benzyl N-<(3aα,12α,12aα,12bα)-1,2,3,3a,4,5,11,12,12a,12b-decahydro-3aα-ethyl-5-oxoisoquino<2,1,8-lma>carbazol-12-yl>carbamate
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 1.) NaH / 1.) DMF, RT, 30 min, 2.) DMF, 0.5 h
2: 74.6 percent / 1,3,5-trimethyl-benzene / 20 h / Heating
3: 97.7 percent / HCl / ethanol; dioxane / 0.5 h / Heating
4: 89.6 percent / aq. KOH / methanol / 0.5 h / Heating
5: diphenylphosphoryl azide, triethylamine / toluene / 1 h / Heating
6: toluene / 2 h / Heating
With
hydrogenchloride; potassium hydroxide; diphenylphosphoranyl azide; sodium hydride; triethylamine;
In
1,4-dioxane; methanol; ethanol; toluene; 1,3,5-trimethyl-benzene;