Technology Process of 4-(4-iodo-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridine
There total 10 articles about 4-(4-iodo-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridine 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:
-
4-(3,5-dimethylpyridin-4-yl)-3,5-dimethyl-phenylamine;
With
nitrosonium tetrafluoroborate;
In
acetonitrile;
at -30 ℃;
for 1h;
With
sodium iodide;
In
acetonitrile;
at -30 - 20 ℃;
DOI:10.1021/ol051365x
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 92.8 percent / pyridine / 6 h / 20 °C
2.1: 97.7 percent / Cs2CO3; BINAP / Pd(OAc)2 / tetrahydrofuran / 15 h / 65 °C
3.1: 99 percent / NaOAc; NH2OH*HCl / methanol / 1.5 h / 20 °C
4.1: nitrosonium tetrafluoroborate / acetonitrile / 1 h / -30 °C
4.2: 72 percent / NaI / acetonitrile / -30 - 20 °C
With
pyridine; hydroxylamine hydrochloride; sodium acetate; caesium carbonate; nitrosonium tetrafluoroborate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl;
palladium diacetate;
In
tetrahydrofuran; methanol; acetonitrile;
DOI:10.1021/ja0674690
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 91.6 percent / pyridine*HCl / 3 h / 210 °C
2.1: 92.8 percent / pyridine / 6 h / 20 °C
3.1: 97.7 percent / Cs2CO3; BINAP / Pd(OAc)2 / tetrahydrofuran / 15 h / 65 °C
4.1: 99 percent / NaOAc; NH2OH*HCl / methanol / 1.5 h / 20 °C
5.1: nitrosonium tetrafluoroborate / acetonitrile / 1 h / -30 °C
5.2: 72 percent / NaI / acetonitrile / -30 - 20 °C
With
pyridine; hydroxylamine hydrochloride; sodium acetate; pyridine hydrochloride; caesium carbonate; nitrosonium tetrafluoroborate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl;
palladium diacetate;
In
tetrahydrofuran; methanol; acetonitrile;
DOI:10.1021/ja0674690