Technology Process of Benzenedecanal, 3,5-dimethoxy-
There total 13 articles about Benzenedecanal, 3,5-dimethoxy- 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
phosgene; dimethyl sulfoxide; triethylamine;
In
dichloromethane;
at -78 ℃;
DOI:10.1021/jm501846y
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1.) O3, 2.) Et3N / 1.) CH2Cl2, -78 deg C, 2.) CH2Cl2, from -78 deg C to RT
2: 1.) n-BuLi / 1.) THF, hexane, RT, 15 min, 2.) THF, hexane, RT, 18 h
3: 91 percent / H2 / 10percent Pd/C / ethanol / 12 h
4: 94 percent / p-toluenesulfonic acid, H2O / tetrahydrofuran / 18 h / Ambient temperature
5: 1.) (COCl)2, DMSO, 2.) Et3N / 1.) CH2Cl2, -78 deg C, 1 h, 2.) CH2Cl2, 0 deg C, 20 min
With
n-butyllithium; oxalyl dichloride; water; hydrogen; toluene-4-sulfonic acid; ozone; dimethyl sulfoxide; triethylamine;
palladium on activated charcoal;
In
tetrahydrofuran; ethanol;
DOI:10.1248/cpb.41.561
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 1.) n-BuLi / 1.) THF, hexane, RT, 15 min, 2.) THF, hexane, RT, 18 h
2: 91 percent / H2 / 10percent Pd/C / ethanol / 12 h
3: 94 percent / p-toluenesulfonic acid, H2O / tetrahydrofuran / 18 h / Ambient temperature
4: 1.) (COCl)2, DMSO, 2.) Et3N / 1.) CH2Cl2, -78 deg C, 1 h, 2.) CH2Cl2, 0 deg C, 20 min
With
n-butyllithium; oxalyl dichloride; water; hydrogen; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine;
palladium on activated charcoal;
In
tetrahydrofuran; ethanol;
DOI:10.1248/cpb.41.561
