Technology Process of Propanoic acid, 2,2-dimethyl-,
(1S,2E)-1-[(4S,5S)-5-[1-hydroxy-3-[(4-methylphenyl)sulfonyl]-2-propynyl]
-2,2-dimethyl-1,3-dioxolan-4-yl]-2,4-pentadienyl ester
There total 6 articles about Propanoic acid, 2,2-dimethyl-,
(1S,2E)-1-[(4S,5S)-5-[1-hydroxy-3-[(4-methylphenyl)sulfonyl]-2-propynyl]
-2,2-dimethyl-1,3-dioxolan-4-yl]-2,4-pentadienyl ester 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
tetrabutyl ammonium fluoride;
In
tetrahydrofuran;
at -78 ℃;
for 1h;
DOI:10.1021/ol034823f
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 91 percent / oxalyl chloride; DMSO / CH2Cl2 / 0.58 h / -78 °C
2.1: n-BuLi / tetrahydrofuran; hexane; hexamethylphosphoric acid triamide / 1 h / -78 °C
2.2: 53 percent / tetrahydrofuran; hexane; hexamethylphosphoric acid triamide / 2 h / -78 °C
3.1: pyridine; DMAP / CH2Cl2 / 12 h / Heating
4.1: 84 percent / tetrabutylammonium fluoride / tetrahydrofuran / 2 h / 20 °C
5.1: 82 percent / oxalyl chloride; DMSO / CH2Cl2 / 0.58 h / -78 °C
6.1: 58 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1 h / -78 °C
With
pyridine; dmap; n-butyllithium; oxalyl dichloride; tetrabutyl ammonium fluoride; dimethyl sulfoxide;
In
tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; dichloromethane;
DOI:10.1021/ol034823f
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: n-BuLi / tetrahydrofuran; hexane; hexamethylphosphoric acid triamide / 1 h / -78 °C
1.2: 53 percent / tetrahydrofuran; hexane; hexamethylphosphoric acid triamide / 2 h / -78 °C
2.1: pyridine; DMAP / CH2Cl2 / 12 h / Heating
3.1: 84 percent / tetrabutylammonium fluoride / tetrahydrofuran / 2 h / 20 °C
4.1: 82 percent / oxalyl chloride; DMSO / CH2Cl2 / 0.58 h / -78 °C
5.1: 58 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1 h / -78 °C
With
pyridine; dmap; n-butyllithium; oxalyl dichloride; tetrabutyl ammonium fluoride; dimethyl sulfoxide;
In
tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; dichloromethane;
DOI:10.1021/ol034823f