HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 22163737, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | (1,3-Dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-7H-purin-7-yl)acetaldehyde | HCID 14482471 | — |
| Reactant | HCID 22163746 | HCID 22163746 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22163737 | HCID 22163737 | 55% |
Reaction Steps
20.8 g 2-(3-methyl-xanthine-7-yl)-acetaldehyde (Formula IV)-prepared similarly like 7-theophyllinyl acetaldehyde Il Farmaco, Ed. Sc. 17, 73; (1962), 40.0 ethylene glycol (Formula II) 2.5 g DOWEX 50 W synthetic resin and 1,000.0 cm3 toluene are heated under stirring in a flask equipped with a water condenser and a cooler until water condensation ceases. The reaction mixture is filtered hot and the precipitate is washed with hot toluene and the filtrate is washed upon cooling with 5% sodium hydrogen carbonate and the organic layer is evaporated after drying. The residue is crystallized three times from propanol and 2-[(3-methyl-xanthine-7-yl)methyl]-1,3-dioxolane is obtained with a yield of 55%, melting point 276°-278° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960773 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-1de6314232d54ea3845a79fcd919390e |
| Source note | uspto-grants-1990_10 |