HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 22281032, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 69733599 | HCID 69733599 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22281032 | HCID 22281032 | 85% |
Reaction Steps
Next, the thus obtained 5-(4-ethoxy-3-buten-1-yl)-2-norbornene was mixed with 90 g of ethylene glycol, 1.0 g of p-toluenesulfonic acid and 300 ml of toluene and heated under reflux for one hour. The reaction mixture was allowed to cool down and poured into 100 ml of saturated sodium bicarbonate water. The resulting mixture separated into two layers. The organic layer was washed with water and saturated sodium chloride water, dried over anhydrous sodium sulfate, and concentrated in vacuum. It was further purified by vacuum distillation, obtaining 177 g of 2-{3-(5-norbornen-2-yl)-1-propyl}-1,3-dioxolane (boiling point 92° C./27 Pa, yield 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06515149B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-6565c6debb194bdaaffe392505f666aa |
| Source note | uspto-grants-2003_02 |