Technology Process of 1-<(3,4-dichlorophenyl)acetyl>-6-(1-pyrrolidinylmethyl)-3-piperidinol
There total 4 articles about 1-<(3,4-dichlorophenyl)acetyl>-6-(1-pyrrolidinylmethyl)-3-piperidinol 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 4 steps
1: 90 percent / etheral HCl, SOCl2 / 4 h / 0 - 20 °C
2: 64 percent / Et3N / CH2Cl2 / 1.) -60 deg C, 1 h, 2.) RT, 72 h
3: 35 percent / H2 / 5percent Rh/C / ethanol / 14 h / 70 °C / 3620.04 Torr
4: 1.) 1,1'-carbonyldiimidazole / 1.) CH2Cl2, RT, 40 min, 2.) CH2Cl2, RT, 18 h
With
hydrogenchloride; thionyl chloride; hydrogen; triethylamine; 1,1'-carbonyldiimidazole;
Rh on carbon;
In
ethanol; dichloromethane;
DOI:10.1021/jm00081a009
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 35 percent / H2 / 5percent Rh/C / ethanol / 14 h / 70 °C / 3620.04 Torr
2: 1.) 1,1'-carbonyldiimidazole / 1.) CH2Cl2, RT, 40 min, 2.) CH2Cl2, RT, 18 h
With
hydrogen; 1,1'-carbonyldiimidazole;
Rh on carbon;
In
ethanol;
DOI:10.1021/jm00081a009
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 64 percent / Et3N / CH2Cl2 / 1.) -60 deg C, 1 h, 2.) RT, 72 h
2: 35 percent / H2 / 5percent Rh/C / ethanol / 14 h / 70 °C / 3620.04 Torr
3: 1.) 1,1'-carbonyldiimidazole / 1.) CH2Cl2, RT, 40 min, 2.) CH2Cl2, RT, 18 h
With
hydrogen; triethylamine; 1,1'-carbonyldiimidazole;
Rh on carbon;
In
ethanol; dichloromethane;
DOI:10.1021/jm00081a009
