Technology Process of 2,3,4,5-tetra-O-methyl-1,6-di-O-trityl-D-mannitol
There total 1 articles about 2,3,4,5-tetra-O-methyl-1,6-di-O-trityl-D-mannitol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
sodium hydride;
In
tetrahydrofuran; mineral oil;
at 25 ℃;
for 25h;
Inert atmosphere;
Reflux;
DOI:10.1021/jo500645z
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 91 percent / H2 / 10 percent Pd/C / methanol; CH2Cl2 / 24 h / 2327.17 Torr
2: 90 percent / 60 percent HNO3 / H2O / 24 h / 70 - 80 °C
3: 18.77 g / DCC; DMAP / CH2Cl2 / 20 °C
With
dmap; hydrogen; nitric acid; dicyclohexyl-carbodiimide;
palladium on activated charcoal;
In
methanol; dichloromethane; water;
DOI:10.1016/S0008-6215(03)00093-4
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: toluene-4-sulfonic acid / dichloromethane; methanol / 18 h
2.1: dimethyl sulfoxide; oxalyl dichloride / dichloromethane / 0.42 h / -78 °C / Inert atmosphere
2.2: 1.5 h / -78 - 25 °C / Inert atmosphere
3.1: triethylamine; 2-pentafluorophenyl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate / 1,2-dichloro-ethane / 16 h / 40 °C / Inert atmosphere
With
2-pentafluorophenyl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate; oxalyl dichloride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine;
In
methanol; dichloromethane; 1,2-dichloro-ethane;
2.1: |Swern Oxidation / 2.2: |Swern Oxidation;
DOI:10.1021/jo500645z