HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-Bromo-4-(1,3-dioxolan-2-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Bromo-4-pyridinecarboxaldehyde | HCID 2762991 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-4-(1,3-dioxolan-2-yl)pyridine | HCID 14696507 | 82% |
Reaction Steps
60 g of 2-bromo-4-pyridinecarboxaldehyde was dissolved in 600 ml of benzene, and 40 g of ethylene glycol and 6 g of p-toluenesulfonic acid were put in the solution. The mixture was heated under reflux for 18 hours while water was removed by using a Dean-Stark trap. After the reaction, the reaction mixture was made basic by adding ice and a saturated aqueous solution of sodium hydrogen carbonate. The organic layer was washed with water and dried. The solvent was evaporated. The residue was distilled to give 60 g (yield 82%) of 2-bromo-4-(1,3-dioxolan-2-yl)pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04977267 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-4404f8a68aec4a05ad8e810df7ebb21c |
| Source note | uspto-grants-1990_12 |