HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-(4-Bromophenyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Bromobenzaldehyde | HCID 81129 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Bromophenyl)-1,3-dioxolane | HCID 2773842 | — |
Reaction Steps
40 g (216 mmol) of bromobenzaldehyde, 39 ml (700 mmol) of ethylene glycol, 1.6 g (9.3 mmol) of p-toluene sulphonic acid and 670 ml of toluene are introduced into a 2 l three-necked flask equipped with a Dean-Stark apparatus under nitrogen. The reaction mixture is taken to reflux whilst eliminating the water formed. After 24 hours of reflux, the reaction mixture is hydrolized with a saturated solution of sodium carbonate (240 ml). The organic phase is recovered and washed twice with a saturated solution of sodium chloride (2×160 ml), then concentrated under vacuum. The crude product obtained is distilled under 40 mm/Hg (150-156° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046352 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-a54c1747fabe4c7894f4cb9f42347a8e |
| Source note | uspto-grants-2000_04 |