Technology Process of 1-Dec-1-en-2-ylsulfonyl-4-methylbenzene
There total 5 articles about 1-Dec-1-en-2-ylsulfonyl-4-methylbenzene 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
sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid;
In
dichloromethane;
for 24h;
Ambient temperature;
DOI:10.1246/cl.1986.341
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 1.) butyllithium (BuLi), HMPA / 1.)THF, hexane, -72 deg C, 30 min; 2.) THF, -72 deg C, 1 h
2: 95 percent / m-chloroperbenzoic acid (MCPBA), sodium hydrocarbonate (NaHCO3) / CH2Cl2 / 24 h / Ambient temperature
With
N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid;
In
dichloromethane;
DOI:10.1246/cl.1986.341
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 253 mg / acetonitrile / 28 h / Ambient temperature
2: 1.) butyllithium (BuLi), HMPA / 1.)THF, hexane, -72 deg C, 30 min; 2.) THF, -72 deg C, 1 h
3: 95 percent / m-chloroperbenzoic acid (MCPBA), sodium hydrocarbonate (NaHCO3) / CH2Cl2 / 24 h / Ambient temperature
With
N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid;
In
dichloromethane; acetonitrile;
DOI:10.1246/cl.1986.341