HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethylene Glycol → 2-(3-Ethenylphenyl)-1,3-dioxolane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethylene Glycol | HCID 174 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 3-Vinylbenzaldehyde | HCID 39390 | — |
| Edukt | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 2-(3-Ethenylphenyl)-1,3-dioxolane | HCID 10241313 | — |
Reaktionsschritte
To a solution of 3-ethenylbenzaldehyde from Step 1 (3.77 g) and ethylene glycol (1.8 mL) in benzene (40 mL) was added p-toluenesulfonic acid monohydrate (100 mg). The reaction mixture was heated to reflux for 6 hours. The water produced by the reaction was collected in a Dean-Stark trap. The reaction was allowed to cool to room temperature. The reaction was diluted with NH4OAc buffer and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and evaporated. Flash chromatography of the residue using 15% diethyl ether in hexane afforded the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05428171 |
| Quelldatensatz | uspto-grants-1995_06 |
| ORD ID | ord-587e164d49264c9ebf8e8b4e81762f69 |
| Quellennotiz | uspto-grants-1995_06 |