Technology Process of Furo[3,2-c]pyridine-3,4-dicarboxylic acid, 2,3-dihydro-, 4-(phenylmethyl)
ester
There total 6 articles about Furo[3,2-c]pyridine-3,4-dicarboxylic acid, 2,3-dihydro-, 4-(phenylmethyl)
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
ruthenium trichloride; sodium periodate;
In
tetrachloromethane; water; acetonitrile;
at 20 ℃;
for 3h;
DOI:10.3987/com-04-s(p)22
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 99 percent / sodium hydride / tetrahydrofuran / 2 h / 0 - 20 °C
2: 90 percent / lithium hydroxide / tetrahydrofuran; H2O / 40 h / 20 °C
3: 91 percent / DCC; DMAP / CH2Cl2 / 20 h / 20 °C
4: 50 percent / tri-n-butyltin hydride; AIBN / toluene / 3 h / 80 °C
5: 32 percent / sodium-periodate; ruthenium chloride / acetonitrile; CCl4; H2O / 3 h / 20 °C
With
dmap; ruthenium trichloride; lithium hydroxide; sodium periodate; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; sodium hydride; dicyclohexyl-carbodiimide;
In
tetrahydrofuran; tetrachloromethane; dichloromethane; water; toluene; acetonitrile;
5: Sharpless-oxidation;
DOI:10.3987/com-04-s(p)22
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 91 percent / DCC; DMAP / CH2Cl2 / 20 h / 20 °C
2: 50 percent / tri-n-butyltin hydride; AIBN / toluene / 3 h / 80 °C
3: 32 percent / sodium-periodate; ruthenium chloride / acetonitrile; CCl4; H2O / 3 h / 20 °C
With
dmap; ruthenium trichloride; sodium periodate; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; dicyclohexyl-carbodiimide;
In
tetrachloromethane; dichloromethane; water; toluene; acetonitrile;
3: Sharpless-oxidation;
DOI:10.3987/com-04-s(p)22