HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-Pentyl-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-Hexanol | HCID 8103 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Pentyl-1,3-dioxolane | HCID 77050 | — |
Reaction Steps
30 g (0.29 mole) of hexanol, 31 g (0.5 mol) of ethylene glycol, 100 mg of p-toluenesulfonic acid (p-Ts) in 100 ml of benzene are placed in 250 ml round-bottomed flask equipped with a Dean-Stark trap, a condenser and a mechanical stirrer. The mixture is heated to reflux until no more water has separated from the benzene phase. The mixture is then cooled to room temperature, washed with 100 ml of 5% sodium bicarbonate, 100 ml of saturated NaCl solution, and finally water. The solution is dried over sodium sulfate. After removing the solvent, the oil is fractionated. A yield of 19.6 g of colorless oil (46%) is obtaind nD20 =1.4554.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04861764 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-4278137c5fb74690991bda9b47b61e3c |
| Source note | uspto-grants-1989_08 |